510(k) K051214 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ALUMA SKIN RENEWAL SYSTEM
| Applicant | Lumenis, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Oct 24, 2005 |
| Received | May 12, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051214
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.