510(k) K220877 ยท HQF Laser, Ophthalmic
Selecta Duet LED, Digital Duet, Selecta LED Trio, Digital Trio Laser Systems
| Applicant | Lumenis Be, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 15, 2022 |
| Received | Mar 25, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220877
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.