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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Tube, Tracheal (W/Wo Connector)
510(k) Number K790312
Device Name ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR
Applicant
RESPIRATORY SUPPORT PRODUCTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
RESPIRATORY SUPPORT PRODUCTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.5730
Classification Product Code
BTR  
Date Received02/13/1979
Decision Date 02/21/1979
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
Recalls CDRH Recalls
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