510(k) K030147 ยท GEX Powered Laser Surgical Instrument
LUMENIS FAMILY OF ULTRAPULSE SURGITOUCH CO2 SURGICAL LASERS
| Applicant | Lumenis, Ltd., Santa Clara CA, US |
| Decision | Substantially Equivalent, Apr 15, 2003 |
| Received | Jan 15, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030147
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.