510(k) K120567 ยท FAS Electrode, Electrosurgical, Active, Urological
GYRUS AMCI PK BUTTON ELECTRODE
| Applicant | Gyrus Acmi, Inc., Southborough MA, US |
| Decision | Substantially Equivalent, Jun 20, 2012 |
| Received | Feb 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120567
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.