Ncontact Surgical, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K142084 | EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX | October 28, 2014 |
| K120857 | EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX | November 13, 2012 |
| K090202 | NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123 AND -125 | February 17, 2009 |
| K082203 | NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025 | December 30, 2008 |
| K071819 | NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515 | July 26, 2007 |
| K062539 | NCONTACT COAGULATION SYSTEM KIT | December 1, 2006 |
| K063012 | NCONTACT COAGULATION SYSTEM KIT, MODEL CSK | December 1, 2006 |