Micomed GmbH
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) | K991862 | MICOMED POSTERIOR DOUBLEROD SYSTEM (MPDS) | MNI | 2000-01-13 | View |
| 510(k) | K982006 | MICOMED - HALM ZIELKE INSTRUMENTATION | KWQ | 1999-01-20 | View |
No matching devices.
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