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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 K760787
Device Name LIBERATOR/STROLLER
Applicant
Burditt & Calkins-Siemens-Elema
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Burditt & Calkins-Siemens-Elema
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number868.5655
Classification Product Code
BYJ  
Date Received10/06/1976
Decision Date 10/22/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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