510(k) K020778 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
GYRUS ENT SOMNOPLASTY TISSUE COAGULATING ELECTRODE, MODEL 2420
| Applicant | Gyrus Ent LLC, Bartlett TN, US |
| Decision | Substantially Equivalent, May 28, 2002 |
| Received | Mar 11, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020778
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.