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Sign in to claim this brandPARKS MEDICAL ELECTRONICS, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 19460 SW SHAW ST, ALOHA, OR, 97007
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3020115
- DUNS Number
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Catalogue (436)
Page 4 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Doppler Model 841-A W/Adult | 841-A CE-1 | FDA UDI | Class II | Active |
| 9.4mhz Skny Pen Probe 10' | 832-2940-41 | FDA UDI | Class II | Active |
| 9.0MHZ Pencil Probe 7FT Contoured | 832-1900-33 | FDA UDI | Class II | Active |
| 9.5mhz Pencil Probe | 832-1950-11 | FDA UDI | Class II | Active |
| Pocket Doppler Model 840 | 840 NV | FDA UDI | Class II | Active |
| 8.3mhz Infant Flat Probe 841-A | 832-4830-21 | FDA UDI | Class II | Active |
| 9.6 Pencil Probe 840 | 832-7960-01 | FDA UDI | Class II | Active |
| 18-B Ir Remote Receiver | 300-0277-01 | FDA UDI | Class II | Active |
| 8.3mhz Microvascular Probe | 832-1834-11 | FDA UDI | Class II | Active |
| 9.7mhz Microvascular Probe | 832-1974-11 | FDA UDI | Class II | Active |
| Doppler Model 909 24v | 909 24V UN | FDA UDI | Class II | Active |
| 8.0mhz Adult Flt Probe 841/842 | 832-7802-21 | FDA UDI | Class II | Active |
| 7.9mhz Pencil Probe 841-A | 832-1790-21 | FDA UDI | Class II | Active |
| 8.4mhz Pencil Probe 7' | 832-1840-31 | FDA UDI | Class II | Active |
| 8.1mhz Adult Flat Probe 7' | 832-3810-31 | FDA UDI | Class II | Active |
| 8.2mhz Infant Flat Probe | 832-4820-11 | FDA UDI | Class II | Active |
| 8.3MHz PENCIL PROBE 7' SHLD | 832-1830-32 | FDA UDI | Class II | Active |
| PPG Probe 6FT 3IN, Yellow Housing | 832-8000-20 | FDA UDI | Class II | Active |
| 4b-Sv Corded Remote | 300-0218-01 | FDA UDI | Class II | Active |
| 8.1mhz Adult Flat Probe | 832-3810-11 | FDA UDI | Class II | Active |
| Pocket Doppler Model 842 | 842 | FDA UDI | Class II | Active |
| 8.9mhz Skny Pen Probe | 832-2890-11 | FDA UDI | Class II | Active |
| Doppler Model 1058-C W/Ppg | 1058-C | FDA UDI | Class II | Active |
| 9.9mhz Pencil Probe | 832-1990-11 | FDA UDI | Class II | Active |
| 9.2mhz Adult Flat Probe | 832-3920-11 | FDA UDI | Class II | Active |
| 9.2mhz Avian Infant | 832-0920-11 | FDA UDI | Class II | Active |
| 9.4mhz Adult Flat Probe | 832-3940-11 | FDA UDI | Class II | Active |
| 9.3mhz Pencil Probe 840 | 832-7930-01 | FDA UDI | Class II | Active |
| 8.1mhz Infant Flat Probe 841-A | 832-4810-21 | FDA UDI | Class II | Active |
| 7.9mhz Pencil Probe | 832-1790-11 | FDA UDI | Class II | Active |
| 9.0mhz Skny Pen Probe 10' | 832-2900-41 | FDA UDI | Class II | Active |
| 811-B 24v Sales Kit W/901cc | 811-B 24V 901CC | FDA UDI | Class II | Active |
| 8.2mhz Pencil Probe Shielded | 832-1820-12 | FDA UDI | Class II | Active |
| 811-B 24v Foreign Sales Kit | 811-B 24V (F) | FDA UDI | Class II | Active |
| 8.5mhz Infant Flat Probe | 832-4850-11 | FDA UDI | Class II | Active |
| 2.05mhz Precordial Probe | 832-5205-12 | FDA UDI | Class II | Active |
| 9.5mhz Skny Pen Probe 10' | 832-2950-41 | FDA UDI | Class II | Active |
| Doppler Model 806-Cb | 806-CB(F) | FDA UDI | Class II | Active |
| 9.9mhz Skny Pen Probe | 832-2990-11 | FDA UDI | Class II | Active |
| 8.2mhz Infant Flat Probe 841-A | 832-4820-21 | FDA UDI | Class II | Active |
| Remote Control RF 2100 With Pads | 300-0378-01 | FDA UDI | Class II | Active |
| 8.9mhz Microvascular Probe | 832-1894-11 | FDA UDI | Class II | Active |
| 9.6mhz Pencil Probe 841-A | 832-1960-21 | FDA UDI | Class II | Active |
| 9.7mhz Pencil Probe 7' | 832-1970-31 | FDA UDI | Class II | Active |
| 4.2mhz Pencil Probe 10' | 832-1420-41 | FDA UDI | Class II | Active |
| 8.9mhz Skny Pen Probe 10' | 832-2890-41 | FDA UDI | Class II | Active |
| 8.4mhz Pencil Probe | 832-1840-11 | FDA UDI | Class II | Active |
| 5.3mhz Pencil Probe 7' | 832-1530-31 | FDA UDI | Class II | Active |
| 9.4mhz Adult Flat Probe 10' | 832-3940-41 | FDA UDI | Class II | Active |
| 5.2mhz Pencil Probe 10' | 832-1520-41 | FDA UDI | Class II | Active |
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FDA Recalls (5)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Aug 8, 2012 | Z-0443-2013 | — | terminated | Parks Medical Electronics, Inc. was made aware of two incidents where an air supply tube from their PARKS PVR unit was inadvertently connected to an IV in the patient's arm instead of into the blood pressure cuff. |
| Nov 8, 2007 | Z-0672-2008 | — | terminated | Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter. |
| Nov 8, 2007 | Z-0670-2008 | — | terminated | Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter. |
| Nov 8, 2007 | Z-0671-2008 | — | terminated | Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter. |
| Nov 8, 2007 | Z-0673-2008 | — | terminated | Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter. |