510(k) K952681 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
STRYKER HUMMER II MICRODEBRIDER SYSTEM
| Applicant | Stryker Endoscopy, San Jose CA, US |
| Decision | Substantially Equivalent, Jul 20, 1995 |
| Received | Jun 12, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952681
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.