510(k) K953737 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
VL7600 REM PATIENT RETURN ELECTRODE
| Applicant | Valleylab, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Aug 23, 1995 |
| Received | Aug 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953737
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.