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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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020115
- DUNS Number
- —
Catalogue (436)
Page 1 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| 8.2mhz Adult Flt Probe 841/842 | 832-7822-21 | FDA UDI | Class II | Active |
| 2.10mhz Ob Probe 641 | 832-7210-21 | FDA UDI | Class II | Active |
| 9.9mhz Adult Flat Probe | 832-3990-11 | FDA UDI | Class II | Active |
| 4.3mhz Pencil Probe | 832-1430-11 | FDA UDI | Class II | Active |
| 4.1mhz Pencil Probe 10' | 832-1410-41 | FDA UDI | Class II | Active |
| 2.25mhz Precordial Probe | 832-5225-12 | FDA UDI | Class II | Active |
| 9.6mhz Adult Flat Probe 10' | 832-3960-41 | FDA UDI | Class II | Active |
| 9.4mhz Adult Fl Probe 841/842 | 832-7942-21 | FDA UDI | Class II | Active |
| 9.2mhz Adult Flt Probe 841/842 | 832-7922-21 | FDA UDI | Class II | Active |
| 9.3mhz Skny Pen Probe 10' | 832-2930-41 | FDA UDI | Class II | Active |
| 5mhz Pencil Probe 841/842 | 832-7500-21 | FDA UDI | Class II | Active |
| 9.4MHZ Pencil Probe 7FT Contoured | 832-1940-33 | FDA UDI | Class II | Active |
| Doppler 811-Bts 24v For Pmes | 811-BTS 24V NV | FDA UDI | Class II | Active |
| 3.9mhz Pencil Probe 10' | 832-1390-41 | FDA UDI | Class II | Active |
| 8.4mhz Pencil Probe 10' | 832-1840-41 | FDA UDI | Class II | Active |
| 8.3mhz Infant Flat Probe | 832-4830-11 | FDA UDI | Class II | Active |
| 9.3mhz Microvascular Probe | 832-1934-11 | FDA UDI | Class II | Active |
| 7.9mhz Pencil Probe 841/842 | 832-7791-21 | FDA UDI | Class II | Active |
| 811-Bl 24v Foreign & Domestic | 811-BL 24V 800C | FDA UDI | Class II | Active |
| 8.9mhz Pencil Probe 841/842 | 832-7891-21 | FDA UDI | Class II | Active |
| 2.25mhz Ob Probe | 832-6225-11 | FDA UDI | Class II | Active |
| 9.4mhz Pencil Probe 7' | 832-1940-31 | FDA UDI | Class II | Active |
| 4.1mhz Pencil Probe Shielded | 832-1410-12 | FDA UDI | Class II | Active |
| 4.0mhz Pencil Probe | 832-1400-11 | FDA UDI | Class II | Active |
| 8.4mhz Infant Flat Probe | 832-4840-11 | FDA UDI | Class II | Active |
| 9.4mhz Skny Pen Probe 7' | 832-2940-31 | FDA UDI | Class II | Active |
| 8.2mhz Adult Flat Probe 841-A | 832-3820-21 | FDA UDI | Class II | Active |
| 9.4mhz Pencil Probe | 832-1940-11 | FDA UDI | Class II | Active |
| 4.4mhz Pencil Probe | 832-1440-11 | FDA UDI | Class II | Active |
| 8.0mhz Skny Pen Probe 841-A | 832-2800-21 | FDA UDI | Class II | Active |
| 9.5mhz Pencil Probe Shld | 832-1950-12 | FDA UDI | Class II | Active |
| 9.6mhz Pencil Probe | 832-1960-11 | FDA UDI | Class II | Active |
| 8.5mhz Pencil Probe | 832-1850-11 | FDA UDI | Class II | Active |
| 8.6mhz Pencil Probe 7' | 832-1860-31 | FDA UDI | Class II | Active |
| 9.2mhz Skny Pen Probe | 832-2920-11 | FDA UDI | Class II | Active |
| 4.2mhz Pencil Probe 7' | 832-1420-31 | FDA UDI | Class II | Active |
| 811-Bl 24v Foreign & Domestic | 811-BL 24V 901C | FDA UDI | Class II | Active |
| 9.5mhz Infant Flat Probe | 832-4950-11 | FDA UDI | Class II | Active |
| 9.0mhz Pencil Probe 7' | 832-1900-31 | FDA UDI | Class II | Active |
| 8.3mhz Pencil Probe 841/842 | 832-7831-21 | FDA UDI | Class II | Active |
| 9.5mhz Pencil Probe 841/842 | 832-7951-21 | FDA UDI | Class II | Active |
| 2.15mhz Ob Probe | 832-6215-11 | FDA UDI | Class II | Active |
| 8.0mhz Adult Flat Probe 841-A | 832-3800-21 | FDA UDI | Class II | Active |
| 8.4mhz Skny Pen Probe | 832-2840-11 | FDA UDI | Class II | Active |
| 9.0mhz Skny Pen Probe | 832-2900-11 | FDA UDI | Class II | Active |
| 8.1mhz Skny Pen Probe | 832-2810-11 | FDA UDI | Class II | Active |
| 2.15mhz Precordial Probe | 832-5215-12 | FDA UDI | Class II | Active |
| 9.2mhz Pencil Probe | 832-1920-11 | FDA UDI | Class II | Active |
| 8.3mhz Pencil Probe 841-A | 832-1830-21 | FDA UDI | Class II | Active |
| 18-B Refurb. Ir Remote Rec. | 300-0277-25 | 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. |