ClearanceBrief
510(k) K841859 ยท FPA Set, Administration, Intravascular

SECURA SET

ApplicantDiatek, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 3, 1984
ReceivedMay 4, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841859

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.