ClearanceBrief
510(k) K014091 ยท FRN Pump, Infusion

STRYKER PAINPUMP

ApplicantStryker Corp., Kalamazoo MI, US
DecisionSubstantially Equivalent, Dec 31, 2001
ReceivedDec 12, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K014091

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.