ClearanceBrief
510(k) K912419 ยท HFW Clamp, Umbilical

CORDGUARD BLOOD COLLECTION DEVICE

ApplicantO.B. Tech., Inc., Huntington Beach CA, US
DecisionSubstantially Equivalent, Oct 5, 1992
ReceivedMay 31, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912419

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.