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510(k) Premarket Notification

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Device Classification Name monitor, physiological, patient(with arrhythmia detection or alarms)
510(k) NumberK023569
Device NameSIEMENS MULTIVIEW WORKSTATION MODIFICATIONS
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
16 electronics ave.
danvers,  MA  01923
Contactpenelope h greco
Regulation Number870.1025
Classification Product Code
MHX  
Date Received10/24/2002
Decision Date 11/04/2002
Decision substantially equivalent (SE)
Classification Advisory Committee Cardiovascular
Review Advisory Committee Cardiovascular
Statement/Summary/Purged Status Summary/purged 510(k)
summary summary
Type Special
Reviewed by Third Party No
Expedited Review No
 
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