ClearanceBrief
510(k) K050840 ยท JOY Device, Automated Cell-Locating

MODIFICATION TO DUET SYSTEM

ApplicantBioview , Ltd., Ramat-Gan, IL
DecisionSubstantially Equivalent, Aug 16, 2005
ReceivedApr 1, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K050840

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.