ClearanceBrief
510(k) K895102 ยท JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

BIOTRACK PDS MONITOR

ApplicantBiotrack, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Oct 10, 1989
ReceivedAug 15, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895102

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.