510(k) K031249 ยท FRN Pump, Infusion
MODIFICATION TO STRYKER PAINPUMP
| Applicant | Stryker Instruments, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Jul 21, 2003 |
| Received | Apr 18, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031249
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.