Biowave Corporation
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261522 | BioWave BioWraps | GXY | 2026-06-03 | View |
| 510(k) | K203158 | BioWave BioWraps | GXY | 2021-07-08 | View |
| 510(k) | K210202 | BioWaveGO RX | GZJ | 2021-02-24 | View |
| 510(k) | K180943 | BioWaveGO | GZJ | 2018-08-17 | View |
| 510(k) | K072123 | HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE | GZJ | 2008-02-01 | View |
| 510(k) | K061166 | DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM | NHI | 2006-08-15 | View |
| 510(k) | K052289 | DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE | LIH | 2005-12-13 | View |
No matching devices.
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