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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name circuit, breathing (w connector, adaptor, y piece)
510(k) Number K811700
Device Name CIRCUIT, BREATHING
Applicant
MARQUEST MEDICAL PRODUCTS, INC.
112 Inverness Circle
Suite A
Englewood,  CO  80112
Applicant Contact Robert J McKinnon
Correspondent
MARQUEST MEDICAL PRODUCTS, INC.
112 Inverness Circle,
Suite A
Englewood,  CO  80112
Correspondent Contact Robert J McKinnon
Regulation Number868.5240
Classification Product Code
CAI  
Date Received06/16/1981
Decision Date 07/10/1981
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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