510(k) K012631 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
REPROCESSED SOFT TISSUE ABLATORS
| Applicant | Alliance Medical Corp., Phoenix AZ, US |
| Decision | Substantially Equivalent, Dec 6, 2001 |
| Received | Aug 13, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012631
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.