510(k) K030885 ยท FRN Pump, Infusion
MODIFICATION TO STRYKER PAINPUMP2
| Applicant | Stryker Instruments, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Apr 18, 2003 |
| Received | Mar 21, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030885
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.