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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 K041223
Device Name MODIFICATION TO SERVO-I VENTILATOR SYSTEM, MODEL 64 87 800 E407E
Original Applicant
MAQUET CRITICAL CARE AB
1140 route 22 east
suite 202
bridgewater,  NJ  08807
Original Contact jamie yieh
Regulation Number868.5895
Classification Product Code
CBK  
Date Received05/10/2004
Decision Date 07/29/2004
Decision substantially equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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