FDA 510(k) Applications Submitted by ARTIE KAUSHIK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160338 | 02/08/2016 | Triton System | GAUSS SURGICAL INC. |
| K091733 | 06/11/2009 | VASOVIEW 6 PRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-2500 | MAQUET CARDIOVASCULAR, LLC |
| K163507 | 12/14/2016 | Triton Sponge System | Gauss Surgical, Inc. |
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