ClearanceBrief
510(k) K120591 ยท JIT Calibrator, Secondary

DIAMOND TOKYO BOEKI ISE MODULE CALIBRATOR 1,2,1-2

ApplicantDiamond Diagnostics, Inc., Holliston MA, US
DecisionSubstantially Equivalent, Apr 17, 2012
ReceivedFeb 28, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120591

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.