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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 K883159
Device Name OHMEDA 7800 ANESTHESIA VENTILATOR
Original Applicant
OHMEDA MEDICAL
ohmeda drive, p.o. box 7550
madison,  WI  53707 -7550
Original Contact timothy m davis
Regulation Number868.5895
Classification Product Code
CBK  
Date Received07/25/1988
Decision Date 06/06/1989
Decision substantially equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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