Sara Dan, 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) | K792600 | MODEL III HANDSWITCH | GEI | 1980-01-10 | View |
| 510(k) | K790684 | COLOR CODING OF SURGICAL INSTRUMENTS | FZT | 1979-05-18 | View |
No matching devices.
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