510(k) K944476 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
APEX UNIVERSAL DRIVE SYSTEM
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Nov 18, 1994 |
| Received | Sep 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944476
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.