Diversified Diagnostic Industries
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) | K870410 | CHROMAGEN TEST FOR GROUP D ENTEROCOCCUS | JTO | 1987-04-21 | View |
| 510(k) | K870561 | CHROMAGEN TEST FOR GRAM (+) & (-) DIFFERENTIATION | JTO | 1987-04-21 | View |
| 510(k) | K870409 | CHROMAGEN TEST FOR GROUP A STREP | JTO | 1987-04-15 | View |
No matching devices.
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