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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Connector, Airway (Extension)
510(k) Number K931216
Device Name CONNECTORS AND AIRWAY EXTENSIONS
Applicant
TEKNOR MEDICAL PRODUCTS, INC.
P.O. BOX 22017
TRENTON, ONTARIO,  CA K8V 6S3
Applicant Contact PETER F HUFF
Correspondent
TEKNOR MEDICAL PRODUCTS, INC.
P.O. BOX 22017
TRENTON, ONTARIO,  CA K8V 6S3
Correspondent Contact PETER F HUFF
Regulation Number868.5810
Classification Product Code
BZA  
Date Received03/10/1993
Decision Date 04/23/1993
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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