ClearanceBrief
510(k) K912043 ยท CBT Arterial Blood Sampling Kit

ACCU-VENT(TM) WITH NEEDLE-PRO(TM)

ApplicantConcord/Portex, Keene NH, US
DecisionUnknown, Jul 5, 1991
ReceivedMay 8, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912043

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.