510(k) K022060 ยท GEX Powered Laser Surgical Instrument
LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES
| Applicant | Lumenis, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Oct 30, 2002 |
| Received | Jun 25, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022060
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.