ClearanceBrief
510(k) K914620 ยท DQA Oximeter

HMS-4000 PHYSIOLOGICAL MONITOR, MODIFICATION

ApplicantVitalog Monitoring,Inc., Redwood CA, US
DecisionSubstantially Equivalent, May 1, 1992
ReceivedOct 16, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914620

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.