ClearanceBrief
510(k) K080695 ยท FPA Set, Administration, Intravascular

MOBILE I.V. SYSTEMS 10,20,60

ApplicantNorthwind Technologies, Corp., Manchester MI, US
DecisionSubstantially Equivalent, Jul 1, 2008
ReceivedMar 11, 2008
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K080695

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.