FDA 510(k) Applications Submitted by G-Flex Europe SPRL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K211909 | 06/21/2021 | Cysto-Gastro-Sets | G-Flex Europe SPRL |
| K222006 | 07/07/2022 | Sclerotherapy & Endoscopic Needles | G-Flex Europe SPRL |
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