Rapid Acoustic Pulse Device — Soliton, Inc. (510(k) K200331)
Rapid Acoustic Pulse Device — Soliton, Inc. (510(k) K200331) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: Rapid Acoustic Pulse Device; Applicant: Soliton, Inc.; Clearance track: 510(k).
| Device name | Rapid Acoustic Pulse Device |
|---|---|
| Applicant | Soliton, Inc. |
| Clearance track | 510(k) |
| Submission number | K200331 |
| Decision | Substantially Equivalent |
| Decision date | 2020-03-10 |
| Date received | 2020-02-10 |
| Product code | GEX |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | TX, US |
| Source | openFDA device |
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$1999/mo
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