510(k) K092009 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
MODIFICATION TO: LEVEEN SUPERSLIM NEEDLE ELECTRODES, MODELS M001262260, M001262270, M001262280, M001262290
| Applicant | Boston Scientific Corporation, Marlboro MA, US |
| Decision | Substantially Equivalent, Nov 6, 2009 |
| Received | Jul 6, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092009
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.