Pearce Clinical Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K874180 | COLORECTAL CANCER RISK DETECTOR (TM) | KHE | 1988-09-30 | View |
| 510(k) | K864544 | DIABETES RISK DETECTOR | JIL | 1987-07-27 | View |
| 510(k) | K871482 | HYPERTENSION RISK DETECTOR(TM) | DXN | 1987-06-05 | View |
No matching devices.
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