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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Flowmeter, Tube, Thorpe, Back-Pressure Compensated
510(k) Number K862797
Device Name AIRCO 2000 SERIES FLOWMETERS
Applicant
Airco, Inc.
Div. Of The Boc Group Inc.
1501 Harpers Rd.
Virginia Beach,  VA  23454
Applicant Contact LOREN C SMITH
Correspondent
Airco, Inc.
Div. Of The Boc Group Inc.
1501 Harpers Rd.
Virginia Beach,  VA  23454
Correspondent Contact LOREN C SMITH
Regulation Number868.2340
Classification Product Code
CAX  
Date Received07/22/1986
Decision Date 08/08/1986
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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