ClearanceBrief
510(k) K980429 ยท DSI Detector And Alarm, Arrhythmia

HP M2600A VIRIDIA TELEMETRY SYSTEM (FORMERLY KNOWN AS THE HP 2600A OMNI-CARE TELEMETRY SYSTEM)

ApplicantHewlett-Packard Co., Andover MA, US
DecisionSubstantially Equivalent, Sep 9, 1998
ReceivedFeb 4, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980429

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.