ClearanceBrief
510(k) K093910 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

IMPROVACUTER GEL & CLOT ACTIVATOR TUBE

ApplicantGuangzhou Improve Medical Instruments Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Jul 12, 2010
ReceivedDec 22, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093910

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.