510(k) K043173 ยท GEX Powered Laser Surgical Instrument
Q-SWITCHED ND:YAG LASER TREATMENT HEAD FOR THE LUMENIS QUANTUM SERIES
| Applicant | Lumenis, Ltd., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jan 31, 2005 |
| Received | Nov 16, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043173
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.