Cappel Diagnostics, 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) | K872839 | ANTINUCLEAR ANTIBODY TEST | LJM | 1987-10-20 | View |
| 510(k) | K864275 | ANTI-NDNA ANTIBODY TEST KIT | KTL | 1986-12-15 | View |
| 510(k) | K862821 | CAPPEL DIAGNOSTICS ANA KIT | DHN | 1986-08-15 | View |
No matching devices.
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