510(k) K031951 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
TRANSDISCAL SYSTEM (TRANSDISCAL PROBE), MODEL TDP-17-150-6
| Applicant | Baylis Medical Co., Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Sep 11, 2003 |
| Received | Jun 24, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031951
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.