510(k) K002565 ยท GXD Generator, Lesion, Radiofrequency
BAYLIS PAIN MANAGEMENT GENERATOR MODEL: PMG-115 (FOR DOMESTIC USE), PMG-230 (FOR INTERNATIONAL USE)
| Applicant | Baylis Medical Co., Inc., Mississauga, CA |
| Decision | Substantially Equivalent, May 3, 2001 |
| Received | Aug 17, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002565
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.