ClearanceBrief
510(k) K974374 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV

ApplicantOhmeda Medical, Murray Hill NJ, US
DecisionSubstantially Equivalent, Jan 2, 1998
ReceivedNov 20, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K974374

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.