510(k) K024093 ยท GEX Powered Laser Surgical Instrument
MODIFIED LUMENIS FAMILY OF INTENSE PULSED-LIGHT (IPL) AND COMBINATION IPL SYSTEMS AND ND:YAG LASER SYSTEMS
| Applicant | Lumenis, Ltd., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jun 19, 2003 |
| Received | Dec 11, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K024093
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.