510(k) K212502 ยท GEX Powered Laser Surgical Instrument
Resonic Rapid Acoustic Pulse Device
| Applicant | Soliton, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Nov 5, 2021 |
| Received | Aug 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212502
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.