FDA 510(k) Applications Submitted by Serkan Sezer
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180735 | 03/22/2018 | Endomat Select | Karl Storz SE & Co. KG |
| K101619 | 06/09/2010 | WELCH ALLYN 1500 PATIENT MONITOR | SCHILLER AG |
| K162992 | 10/27/2016 | Karl Storz UROMAT E.A.S.I. | KARL STORZ ENDOSCOPY AMERICA, INC |
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