510(k) K943569 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
STRYKER TOTAL PERFORMANCE SYSTEM
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Jan 9, 1995 |
| Received | Jul 22, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943569
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.