ClearanceBrief
510(k) K883813 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE

ApplicantCiba Corning Diagnostics Corp., East Walpole MA, US
DecisionSubstantially Equivalent, Nov 10, 1988
ReceivedSep 8, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883813

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.