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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Detector And Alarm, Arrhythmia
510(k) Number K990972
Device Name HP VIRIDIA COMPONENT MONITORING SYSTEM, HP VIRIDIA CMS 24/26, HP VIRIDIA MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE T
Applicant
Hewlett-Packard GmbH
Herrenberger St. 110-140
Boeblingen,  DE 71034
Applicant Contact EGON PFEIL
Correspondent
Hewlett-Packard GmbH
Herrenberger St. 110-140
Boeblingen,  DE 71034
Correspondent Contact EGON PFEIL
Regulation Number870.1025
Classification Product Code
DSI  
Date Received03/23/1999
Decision Date 04/19/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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