510(k) K802330 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
HI-TEMP LOOPTIP SURGICAL CAUTERY
| Applicant | Medical Products Development, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 12, 1980 |
| Received | Sep 23, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802330
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.