ClearanceBrief
510(k) K883877 ยท DQA Oximeter

BM-103 BATTERY MODULE

ApplicantDatex Division Instrumentarium Corp., Helsinki, Finland, FI
DecisionSubstantially Equivalent, Oct 28, 1988
ReceivedSep 13, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883877

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.