510(k) K971512 ยท FAS Electrode, Electrosurgical, Active, Urological
AMS COAGULOOP RESECTION ELECTRODE
| Applicant | American Medical Systems, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jul 24, 1997 |
| Received | Apr 28, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971512
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.