FDA 510(k) Applications Submitted by Bradford Siff
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210202 | 01/25/2021 | BioWaveGO RX | BioWave Corporation |
| K180943 | 04/10/2018 | BioWaveGO | Biowave Corporation |
| K152437 | 08/27/2015 | BiowaveHOME Neuromodulation Pain Therapy Device | BIOWAVE CORPORATION |
| K203158 | 10/22/2020 | BioWave BioWraps | BioWave Corporation |
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