ClearanceBrief
510(k) K781616 ยท CBT Arterial Blood Sampling Kit

OMNI STIK

ApplicantUnitron Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 8, 1978
ReceivedSep 20, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781616

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.