ClearanceBrief
510(k) K984194 ยท MQS System, Hemodialysis, Access Recirculation Monitoring

HP M2376A DEVICE LINK SYSTEM

ApplicantHewlett-Packard Co., Andover MA, US
DecisionSubstantially Equivalent, Apr 30, 1999
ReceivedNov 23, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K984194

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.