FDA 510(k) Applications Submitted by YVERRE BOBAY

FDA 510(k) Number Submission Date Device Name Applicant
K230133 01/17/2023 Plenity Gelesis Inc.
K131179 04/25/2013 CENTRIMAG PRIMARY CONSOLE (2ND GENERATION); MAG MONITOR THORATEC CORP
K201111 04/27/2020 GentleMax Pro Plus Candela Corporation
K243213 10/03/2024 Self-Forming Magnet (FLEX SFM) GI Windows Inc.
K243482 11/08/2024 Self-Forming Magnet (Flexagon) GI Windows Inc.


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