ClearanceBrief
510(k) K922343 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT

ApplicantTri-Tech, Inc., Durham NC, US
DecisionUnknown, Feb 17, 1994
ReceivedMay 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922343

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.