Omnitech Systems, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K151976 | Omnitech HF Resection Electrodes, Omnitech HF Vaporization Electrode | FAS | 2016-06-27 | View |
| 510(k) | K050454 | OMNITECH FULGURATING ELECTRODE | FAS | 2005-05-27 | View |
| 510(k) | K981463 | OMNITECH RESECTOSCOPE ROLLER ELECTRODE | KNF | 1998-07-17 | View |
| 510(k) | K981464 | OMNITECH RESECTOSCOPE CUTTING LOOP ELECTRODE | KNF | 1998-07-10 | View |
| 510(k) | K964365 | RESECTOSCOPE CUTTING LOOP ELECTRODE | FAS | 1997-04-22 | View |
| 510(k) | K965093 | OMNITECH RESECTOSCOPE ROLLER ELECTRODE | FAS | 1997-03-19 | View |
No matching devices.
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