ClearanceBrief
510(k) K884111 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

PUMPETTE(TM)

ApplicantHelena Laboratories, Beaumont TX, US
DecisionSubstantially Equivalent, Dec 14, 1988
ReceivedSep 29, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884111

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.