510(k) K991314 ยท FAS Electrode, Electrosurgical, Active, Urological
COAGULOOP
| Applicant | American Medical Systems, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jun 29, 1999 |
| Received | Apr 16, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991314
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.