510(k) K031950 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
BAYLIS PAIN MANAGEMENT GENERATOR, MODELS PMG-115-TD AND PMG-230-TD
| Applicant | Baylis Medical Co., Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Jul 17, 2003 |
| Received | Jun 24, 2003 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K031950
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.