ClearanceBrief
510(k) K843813 ยท

INTRAVENOUS START KIT

ApplicantPro-Lab, Inc., Round Rock TX, US
DecisionSubstantially Equivalent, Dec 5, 1984
ReceivedSep 28, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843813

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.