510(k) K072478 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
BAYLIS PAIN MANAGEMENT GENERATOR-TD, MODELS: PMG-115-TD AND PMG-230-TD
| Applicant | Baylis Medical Co., Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Dec 19, 2007 |
| Received | Sep 4, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072478
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.