510(k) K994428 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
E7512 PREMIE REM POLYHESIVE II PATIENT RETURN ELECTRODE
| Applicant | Valleylab, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Mar 7, 2000 |
| Received | Dec 30, 1999 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K994428
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.