Biotech Atlantic, Inc.
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) | K032992 | UNIMARK HOME PREGNANCY TEST DEVICE | LCX | 2003-11-21 | View |
| 510(k) | K013194 | UNIMARK HCG COMBO PREGNANCY TEST | JHI | 2001-10-10 | View |
| 510(k) | K960174 | UNIMARK MIDSTREAM PREGNANCY TEST STICK | LCX | 1996-04-01 | View |
| 510(k) | K941090 | UNISTEP HCG PREGNANCY TEST STRIP | DHA | 1994-06-02 | View |
No matching devices.
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