Neomed 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) | K790043 | TRACOR, CANNULA, BICEPTS BIPOLAR | HIN | 1979-02-08 | View |
| 510(k) | K781810 | ELECTROSURGICAL UNIT 3001-3009 | GEI | 1978-12-20 | View |
| 510(k) | K780118 | ELECTRODE, DISPERSIVE, DISP. NEOPAD | HAM | 1978-02-23 | View |
No matching devices.
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