510(k) K112593 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
STYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM
| Applicant | Stryker Corporation, Kalamazoo MI, US |
| Decision | Substantially Equivalent, May 1, 2012 |
| Received | Sep 7, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112593
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.