510(k) K211722 ยท GEX Powered Laser Surgical Instrument
Laser treatment system , models Nyx plus, Grace plus, Nemesis, Ares
| Applicant | Canadian Pioneer Medical Technology Corporation, Vaughan, CA |
| Decision | Substantially Equivalent, Feb 25, 2022 |
| Received | Jun 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211722
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.