ClearanceBrief
510(k) K003543 ยท FRN Pump, Infusion

STRYKER PAINPUMP PCA

ApplicantStryker Instruments, Kalamazoo MI, US
DecisionSubstantially Equivalent, Jun 5, 2001
ReceivedNov 17, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003543

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.