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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name oximeter
510(k) Number K991661
Device Name SIEMENS MEDICAL INFORMATION BUS (MIB) PROTOCOL CONVERTER
Original Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
16 electronics ave.
danvers,  MA  01923
Original Contact penelope h greco
Regulation Number870.2700
Classification Product Code
DQA  
Date Received05/14/1999
Decision Date 05/28/1999
Decision substantially equivalent (SE)
Classification Advisory Committee Anesthesiology
Review Advisory Committee Anesthesiology
summary summary
Type Special
Reviewed by Third Party No
Expedited Review No
Combination Product No
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