HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. K

Detector And Alarm, Arrhythmia

HEWLETT-PACKARD GMBH

The following data is part of a premarket notification filed by Hewlett-packard Gmbh with the FDA for Hp Viridia Component Monitoring System, Model Rev. K.

Pre-market Notification Details

Device IDK990125
510k NumberK990125
Device Name:HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. K
ClassificationDetector And Alarm, Arrhythmia
Applicant HEWLETT-PACKARD GMBH HERRENBERGER STR. 110-140 Boeblingen,  DE 71034
ContactEgon Pfeil
CorrespondentEgon Pfeil
HEWLETT-PACKARD GMBH HERRENBERGER STR. 110-140 Boeblingen,  DE 71034
Product CodeDSI  
CFR Regulation Number870.1025 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received1999-01-13
Decision Date1999-01-29
Summary:summary

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