510(k) K050753 ยท FMF Syringe, Piston
STRYKER DISCMONITOR
| Applicant | Stryker Instruments, Kalamazoo MI, US |
| Decision | Substantially Equivalent, May 18, 2005 |
| Received | Mar 23, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050753
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.