FDA 510(k) Applications Submitted by JANE RICUPERO
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090202 |
01/27/2009 |
NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123 AND -125 |
NCONTACT SURGICAL, INC. |
| K120857 |
03/21/2012 |
EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX |
NCONTACT SURGICAL, INC. |
| K071819 |
07/03/2007 |
NCONTACT VISITRAX GUIDED COAGULATION SYSTEM KIT, MODELS CSK-212 AND CSK-515 |
NCONTACT SURGICAL, INC. |
| K142084 |
07/31/2014 |
EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX |
NCONTACT SURGICAL, INC. |
| K082203 |
08/05/2008 |
NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025 |
NCONTACT SURGICAL, INC. |
| K062539 |
08/29/2006 |
NCONTACT COAGULATION SYSTEM KIT |
NCONTACT SURGICAL, INC. |
| K063012 |
10/02/2006 |
NCONTACT COAGULATION SYSTEM KIT, MODEL CSK |
NCONTACT SURGICAL, INC. |
|
|
