ClearanceBrief
510(k) K993587 ยท MQS System, Hemodialysis, Access Recirculation Monitoring

HP M2376A DEVICE LINK SYSTEM

ApplicantHewlett-Packard Co., Andover MA, US
DecisionSubstantially Equivalent, Jan 20, 2000
ReceivedOct 22, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993587

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.