510(k) K093181 ยท FAS Electrode, Electrosurgical, Active, Urological
GYRUS ACMI PK BUTTON ELECTRODE
| Applicant | Gyrus Acmi, Inc., Southborough MA, US |
| Decision | Substantially Equivalent, Feb 24, 2010 |
| Received | Oct 8, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093181
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.