FDA 510(k) Applications Submitted by JULIE BODMER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K123111 | 10/03/2012 | V8 TRANSLUMINAL BAV CATHETER | INTERVALVE, INC |
| K133607 | 11/25/2013 | V8 TRANSLUMINAL BAV CATHETER | INTERVALVE, INC |
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