510(k) K013369 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
RESECTION ABLATOR
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Apr 4, 2002 |
| Received | Oct 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013369
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.