Ncontact Surgical, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Ncontact Surgical, Inc. — FDA 510(k) Products and Clearance History Cardiovascular ✕
6 devices
Cleared
Oct 28, 2014
EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX
Cardiovascular
89d
Cleared
Nov 13, 2012
EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX
Cardiovascular
237d
Cleared
Feb 17, 2009
NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123...
Cardiovascular
21d
Cleared
Dec 30, 2008
NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021
Cardiovascular
147d
Cleared
Jul 26, 2007
NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515
Cardiovascular
23d
Cleared
Dec 01, 2006
NCONTACT COAGULATION SYSTEM KIT, MODEL CSK
Cardiovascular
60d