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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 K902084
Device Name OHMEDA 7800 ANESTHESIA VENTILATOR SOFTWARE UPDATE
Original Applicant
OHMEDA MEDICAL
ohmeda drive, p.o. box 7550
madison,  WI  53707 7550
Original Contact m davis
Regulation Number868.5895
Classification Product Code
CBK  
Date Received05/08/1990
Decision Date 10/01/1990
Decision substantially equivalent (SE)
Classification Advisory Committee Anesthesiology
Review Advisory Committee Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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