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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name conserver, oxygen
510(k) Number K853378
Device Name AUTO PRO
Applicant
RESPIRATION TECHNOLOGY, INC.
4347 EAST COLFAX AVE.
DENVER,  CO  80220
Applicant Contact LORETTA BOCAST
Correspondent
RESPIRATION TECHNOLOGY, INC.
4347 EAST COLFAX AVE.
DENVER,  CO  80220
Correspondent Contact LORETTA BOCAST
Regulation Number868.5905
Classification Product Code
NFB  
Date Received08/12/1985
Decision Date 09/19/1985
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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