Azog, 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) | K041748 | AZOG, INC. HCG ONE-STEP URINE HOME PREGNANCY TEST (DIP STICK, CASSETTE AND MIDSTREAM) | LCX | 2004-08-09 | View |
| 510(k) | K022680 | AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST STRIP (DIPSTICK) | DHA | 2002-11-01 | View |
| 510(k) | K022681 | AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST (DEVICE OR CASSETTE) | DHA | 2002-11-01 | View |
No matching devices.
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