Dytek Corp.
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) | K781245 | LUNG EXER. BAG, POST-OP, MODIFIED | BWF | 1978-09-20 | View |
| 510(k) | K760168 | PENCIL, ELECTROSURGICAL | GEI | 1976-08-09 | View |
| 510(k) | K760167 | BAG, POST OPERATIVE LUNG EXERCIZING BLOW | BWF | 1976-08-06 | View |
No matching devices.
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