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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name apparatus, suction, ward use, portable, ac-powered
510(k) Number K791241
Device Name BRIOX MODEL 2000-CA COMPRESSOR UNIT
Applicant
BRIOX TECHNOLOGIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
BRIOX TECHNOLOGIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4780
Classification Product Code
JCX  
Date Received07/06/1979
Decision Date 07/24/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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