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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 K896897
Device Name VENTLAB ANESTHESIA CIRCUIT AC 6000
Applicant
VENTLAB CORP.
221 GRACIE PLACE
HACKENSACK,  NJ  07601
Applicant Contact GREGORY LAU
Correspondent
VENTLAB CORP.
221 GRACIE PLACE
HACKENSACK,  NJ  07601
Correspondent Contact GREGORY LAU
Regulation Number868.5240
Classification Product Code
CAI  
Date Received12/08/1989
Decision Date 01/26/1990
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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