Cimed Intl., Inc.
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) | K840766 | JANACEK TUBO-UTERINE IMPLANTATION SET | HTD | 1984-04-23 | View |
| 510(k) | K833676 | SURGICAL VESSEL DILATORS-CATHERIZA- | DWP | 1984-03-19 | View |
| 510(k) | K833629 | CERTAIN MANUAL SURG. INSTRU. ACCESS | HTD | 1984-01-30 | View |
No matching devices.
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