510(k) K894602 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
B1 FOOTSWITCH (SINGLE PEDDLE), B2 (DOUBLE PEDDLE)
| Applicant | Beacon Laboratories, Inc., Westminster CO, US |
| Decision | Substantially Equivalent, Aug 9, 1989 |
| Received | Jul 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894602
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.