ClearanceBrief
510(k) K000822 ยท DSI Detector And Alarm, Arrhythmia

AGILENTCOMPONENT MONITORING SYSTEM, AGILENT 24/26, AGILENT MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE PATIENT MONITOR

ApplicantAgilent Technologies, GmbH, Boeblingen, DE
DecisionSubstantially Equivalent, Apr 6, 2000
ReceivedMar 14, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K000822

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.