FDA 510(k) Applications Submitted by InterValve, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150343 | 02/11/2015 | V8 Transluminal BAV Catheter | InterValve, Inc. |
| K152150 | 08/03/2015 | V8 Balloon Aortic Valvuloplasty Catheter | InterValve, Inc. |
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