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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 K800742
Device Name LIBERATOR/STROLLER II SYSTEM
Applicant
CRYOGENIC ASSOC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
CRYOGENIC ASSOC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number868.5655
Classification Product Code
BYJ  
Date Received04/03/1980
Decision Date 05/23/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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