510(k) K012018 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910
| Applicant | Acmi Corporation, Southborough MA, US |
| Decision | Substantially Equivalent, Jul 16, 2002 |
| Received | Jun 28, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012018
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.