ClearanceBrief
510(k) K770572 ยท JJJ Counter (Beta, Gamma) For Clinical Use

DP-5000 DATA REDUCTION SYSTEM

ApplicantBeckman Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 15, 1977
ReceivedMar 25, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770572

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.