510(k) K981188 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ELECTROSURGICAL CAUTERY PROBES
| Applicant | Microline Pentax, Inc., Wellesley MA, US |
| Decision | Substantially Equivalent, May 20, 1998 |
| Received | Apr 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981188
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.