ClearanceBrief
510(k) K760424 ยท JJJ Counter (Beta, Gamma) For Clinical Use

LIQUID SCINTILLATION COUNTER

ApplicantBeckman Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 2, 1976
ReceivedAug 12, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760424

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.