510(k) K902232 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
WECK ELECTROSURGICAL GENERATOR #174200
| Applicant | Edward Weck, Inc., Research Triangle Pa NC, US |
| Decision | Substantially Equivalent, Aug 2, 1990 |
| Received | May 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902232
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.