Ncontact Surgical, Inc.
Ncontact Surgical, Inc. holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2014.
Top product codes for Ncontact Surgical, Inc.
Recent clearances by Ncontact Surgical, Inc.
- K142084 — EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX
- K120857 — EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX
- K090202 — NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123 AND -125
- K082203 — NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021; CSK-022; CSK-023; CSK-025
- K071819 — NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515
- K062539 — NCONTACT COAGULATION SYSTEM KIT
- K063012 — NCONTACT COAGULATION SYSTEM KIT, MODEL CSK
Data sourced from openFDA. This site is unofficial and independent of the FDA.