ClearanceBrief
510(k) K023098 ยท MEB Pump, Infusion, Elastomeric

ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KIT, ACCUFUSER INFUSION KIT

ApplicantMckinley Infuser, San Francisco CA, US
DecisionSubstantially Equivalent, Dec 9, 2002
ReceivedSep 18, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023098

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.