De Ferris Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K880433 | CYTOMEGALOVIRUS IGG EIA KIT | LFZ | 1989-03-27 | View |
| 510(k) | K875258 | TOXOPLASMA GONDII IGG ELISA KIT | LGD | 1988-09-30 | View |
No matching devices.
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