Company ยท US
Ncontact Surgical, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2006 to 2014. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 28, 2014 | K142084 | EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX Ncontact Surgical, Inc. | OCL |
| Nov 13, 2012 | K120857 | EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX Ncontact Surgical, Inc. | OCL |
| Feb 17, 2009 | K090202 | NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123 AND -125 Ncontact Surgical, Inc. | OCL |
| Dec 30, 2008 | K082203 | NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025 Ncontact Surgical, Inc. | OCL |
| Jul 26, 2007 | K071819 | NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515 Ncontact Surgical, Inc. | OCL |
| Dec 1, 2006 | K063012 | NCONTACT COAGULATION SYSTEM KIT, MODEL CSK Ncontact Surgical, Inc. | OCL |
| Dec 1, 2006 | K062539 | NCONTACT COAGULATION SYSTEM KIT Ncontact Surgical, Inc. | GEI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||