510(k) K031001 ยท FAS Electrode, Electrosurgical, Active, Urological
ACMI VISTA CTR BIPOLAR LOOP ELECTRODE
| Applicant | Acmi Corporation, Southborough MA, US |
| Decision | Substantially Equivalent, May 21, 2003 |
| Received | Mar 31, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031001
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.