510(k) K944244 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
MODEL E278OR-ASP SERIES RETRACTABLE
| Applicant | Valleylab, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Nov 30, 1994 |
| Received | Sep 1, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944244
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.