510(k) K030720 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ULTRABLATOR ELECTRODE
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Jun 3, 2003 |
| Received | Mar 7, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030720
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.