510(k) K083281 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
EL LIGHTWAVE SUCTION ABLATOR, MODEL EL-2000-S, LIGHTWAVE SUCTION ABLATOR, MODEL IA-2000-S, LIGHTWAVE ABLATOR, MODEL IA-
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Feb 25, 2009 |
| Received | Nov 7, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083281
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.