FDA 510(k) Applications Submitted by BEMER Int. AG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210174 | 01/22/2021 | BEMER Therapy Systems, BEMER Classic Set, BEMER Pro-Set | Bemer INT. AG |
| K223919 | 12/29/2022 | B.Light Clear Evo and B.Light Restore Evo | Bemer INT. AG |
| K151834 | 07/06/2015 | BEMER Classic Set, BEMER Pro-Set | BEMER Int. AG |
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