510(k) K962653 ยท FAS Electrode, Electrosurgical, Active, Urological
MICROGYN RESECTION LOOP, COAGULATING ELECTRODE, CISS SHEATH ELECTRODE, LOOP ELECTRODE KIT AND COAGULATING ELECTRODE KIT
| Applicant | Microgyn Corp., Taunton MA, US |
| Decision | Substantially Equivalent, Feb 4, 1997 |
| Received | Jul 8, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962653
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.