ClearanceBrief
510(k) K001333 ยท DSI Detector And Alarm, Arrhythmia

AGILENT COMPONENT MONITORING SYSTEM, AGILENT MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE PATIENT MONITOR, AGILENT NONI

ApplicantAgilent Technologies Deutschland GmbH, Boeblingen,, DE
DecisionSubstantially Equivalent, May 17, 2000
ReceivedApr 27, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K001333

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.