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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name ventilator, continuous, facility use
510(k) Number K960168
Device Name SIEMENS SERVO SCREEN 390 AND SERVO COMPUTER MODULE 990
Original Applicant
SIEMENS ELEMA AB
49 plain st.
north attleboro,  MA  02760
Original Contact steven clarke
Regulation Number868.5895
Classification Product Code
CBK  
Date Received01/16/1996
Decision Date 10/25/1996
Decision se subject to tracking reg (ST)
Classification Advisory Committee Anesthesiology
Review Advisory Committee Anesthesiology
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
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