Eppendorf-Brinkmann, 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) | K780819 | GLYCOHEMOGLOBIN-SKREEN TEST KIT | LCP | 1978-11-07 | View |
| 510(k) | K772337 | URINARY 17-KETOSTERIOD/17 | CDG | 1978-01-12 | View |
| 510(k) | K772151 | URINARY VMA - SCREEN TEST KIT | CDF | 1977-11-30 | View |
| 510(k) | K761271 | URIN. L7-OH CORTICOSTEROID T(NON HYDRO) | CDB | 1977-02-14 | View |
No matching devices.
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