FDA 510(k) Applications Submitted by KARUNA VELUSAMY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100789 | 03/22/2010 | MODIFICATON TO: STEERABLE GUIDE CATHETER, MODEL SGC01ST | EVALVE INC |
| K083793 | 12/22/2008 | STEERABLE GUIDE CATHETER | EVALVE INC |
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