Hyman, Phelps & McNamara, P.C.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K950530 | PRO-TEC-CASE | LRX | 1995-04-07 | View |
| 510(k) | K950878 | MENICON SP VIAL | LRX | 1995-04-07 | View |
| 510(k) | K945834 | PROPHY PRO. | EGS | 1995-02-13 | View |
| 510(k) | K915574 | COMFORT PERSONAL LUBRICANT | KMJ | 1993-02-19 | View |
No matching devices.
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