Ncontact Surgical, 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) | K120857 | EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX | OCL | 2012-11-13 | View |
| 510(k) | K090202 | NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123 AND -125 | OCL | 2009-02-17 | View |
| 510(k) | K082203 | NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025 | OCL | 2008-12-30 | View |
| 510(k) | K071819 | NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515 | OCL | 2007-07-26 | View |
| 510(k) | K063012 | NCONTACT COAGULATION SYSTEM KIT, MODEL CSK | OCL | 2006-12-01 | View |
| 510(k) | K062539 | NCONTACT COAGULATION SYSTEM KIT | GEI | 2006-12-01 | View |
No matching devices.
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