ClearanceBrief
510(k) K063357 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES

ApplicantGreiner Bio-One North America, Inc., Baldwin MD, US
DecisionSubstantially Equivalent, Jul 10, 2007
ReceivedNov 7, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K063357

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.