510(k) K952161 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
BIPOLAR COAGULATION INSTRUMENT
| Applicant | Johnson & Johnson Professionals, Inc., Raritan NJ, US |
| Decision | Substantially Equivalent, Jul 5, 1995 |
| Received | May 8, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952161
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.