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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name unit, liquid-oxygen, portable
510(k) Number K812536
Device Name LINDE MARK II
Applicant
UNION CARBIDE CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
UNION CARBIDE CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.5655
Classification Product Code
BYJ  
Date Received09/03/1981
Decision Date 09/23/1981
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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