ClearanceBrief
510(k) K874198 ยท DQA Oximeter

VITALOG HMS-3000

ApplicantVitalog Corp., Redwood CA, US
DecisionSubstantially Equivalent, Mar 22, 1988
ReceivedOct 9, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874198

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.