ClearanceBrief
510(k) K892665 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

PRO-JECT(TM) SAFETY NEEDLE HOLDER

ApplicantPro-Tec Containers, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Oct 4, 1989
ReceivedApr 13, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K892665

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.