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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Vaporizer, Anesthesia, Non-Heated
510(k) Number K882500
Device Name VAPORIZER, ANESTHESIA, NON-HEATED
Applicant
ANESTHETIC VAPORIZER SERVICES
10185 MAIN ST.
CLARENCE,  NY  14031 -2044
Applicant Contact KEITH JONES
Correspondent
ANESTHETIC VAPORIZER SERVICES
10185 MAIN ST.
CLARENCE,  NY  14031 -2044
Correspondent Contact KEITH JONES
Regulation Number868.5880
Classification Product Code
CAD  
Date Received06/17/1988
Decision Date 08/01/1988
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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