Ncontact Surgical, Inc.
FDA 510(k) medical device clearances.
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.