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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 3 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| 2.15mhz Ob Probe 641-A | 832-6215-21 | FDA UDI | Class II | Active |
| 8.0mhz Pencil Probe | 832-1800-11 | FDA UDI | Class II | Active |
| 9.7mhz Pencil Probe Shld 7' | 832-1970-32 | FDA UDI | Class II | Active |
| 8.1mhz Pencil Probe 10' | 832-1810-41 | FDA UDI | Class II | Active |
| 8.8mhz Pencil Probe | 832-1880-11 | FDA UDI | Class II | Active |
| 8.2mhz Adult Flat Probe | 832-3820-11 | FDA UDI | Class II | Active |
| 9.8mhz Infant Flat Probe | 832-4980-11 | FDA UDI | Class II | Active |
| 8.8mhz Skny Pen Probe | 832-2880-11 | FDA UDI | Class II | Active |
| 9.2mhz Adult Flat Probe 841-A | 832-3920-21 | FDA UDI | Class II | Active |
| 9.7mhz Pencil Probe | 832-1970-11 | FDA UDI | Class II | Active |
| 9.0mhz Infant Fl Probe 841/842 | 832-7900-21 | FDA UDI | Class II | Active |
| 9.8mhz Adult Flat Probe | 832-3980-11 | FDA UDI | Class II | Active |
| 5.1mhz Pencil Probe 841/842 | 832-7510-21 | FDA UDI | Class II | Active |
| Doppler Model 812 110v Foreign | 812-1-F 110V | FDA UDI | Class II | Active |
| 8.6mhz Pencil Probe 841-A | 832-1860-21 | FDA UDI | Class II | Active |
| 8.2mhz Skny Pen Probe | 832-2820-11 | FDA UDI | Class II | Active |
| 9.5mhz Avian Infant | 832-0950-11 | FDA UDI | Class II | Active |
| Doppler Model 842 | 842(F) | FDA UDI | Class II | Active |
| 4.1mhz Pencil Probe 7' | 832-1410-31 | FDA UDI | Class II | Active |
| 9.5mhz Pencil Probe 7' | 832-1950-31 | FDA UDI | Class II | Active |
| 8.8mhz Microvascular Probe | 832-1884-11 | FDA UDI | Class II | Active |
| 2.25mhz Precordial Probe 10' | 832-5225-42 | FDA UDI | Class II | Active |
| 9.1mhz Pencil Probe 841-A | 832-1910-21 | FDA UDI | Class II | Active |
| 8.0mhz Pencil Probe 841-A | 832-1800-21 | FDA UDI | Class II | Active |
| 8.1mhz Skny Pen Probe 7' | 832-2810-31 | FDA UDI | Class II | Active |
| 8.0mhz Infant Flat Probe | 832-4800-11 | FDA UDI | Class II | Active |
| 9.7mhz Pencil Probe 10' | 832-1970-41 | FDA UDI | Class II | Active |
| 9.4mhz Pencil Probe 841-A | 832-1940-21 | FDA UDI | Class II | Active |
| 8.2mhz Pencil Probe 7' | 832-1820-31 | FDA UDI | Class II | Active |
| 8.7mhz Pencil Probe 841-A | 832-1870-21 | FDA UDI | Class II | Active |
| 8.5mhz Adult Flat Probe | 832-3850-11 | FDA UDI | Class II | Active |
| 9.4mhz Microvascular Probe | 832-1944-11 | FDA UDI | Class II | Active |
| 8.0mhz Pencil Probe 841/842 | 832-7801-21 | FDA UDI | Class II | Active |
| 8.5mhz Pencil Probe 7' | 832-1850-31 | FDA UDI | Class II | Active |
| 8.1mhz Infant Fl Probe 841/842 | 832-7813-21 | FDA UDI | Class II | Active |
| 9.1mhz Pencil Probe 840 | 832-7910-01 | FDA UDI | Class II | Active |
| 8.0mhz Skny Pen Probe | 832-2800-11 | FDA UDI | Class II | Active |
| 4.0mhz Pencil Probe 10' | 832-1400-41 | FDA UDI | Class II | Active |
| 8.4mhz Adult Flat Probe | 832-3840-11 | FDA UDI | Class II | Active |
| 10mhz Pencil Probe 840 | 832-7000-01 | FDA UDI | Class II | Active |
| Vas./Ob Doppler Model 917 24v | 917 24V | FDA UDI | Class II | Active |
| 9.6mhz Adult Flat Probe 841-A | 832-3960-21 | FDA UDI | Class II | Active |
| 9.6mhz Pencil Probe Shielded | 832-1960-12 | FDA UDI | Class II | Active |
| 2.75 Mhz Ob Probe | 832-6275-11 | FDA UDI | Class II | Active |
| 8.9mhz Pencil Probe 841-A | 832-1890-21 | FDA UDI | Class II | Active |
| 9.1mhz Skny Pencil | 832-2910-11 | FDA UDI | Class II | Active |
| Doppler Model 812 In 901 C/C | 812-1-901 CC | FDA UDI | Class II | Active |
| 9.7mhz Adult Flat Probe 7' | 832-3970-31 | FDA UDI | Class II | Active |
| 8.0mhz Pencil Probe 7' | 832-1800-31 | FDA UDI | Class II | Active |
| 9.8mhz Pencil Probe 841-A | 832-1980-21 | FDA UDI | Class II | Active |
Related Companies
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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. |