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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheters, Suction, Tracheobronchial
510(k) Number K850105
Device Name KM PRODUCTS ASPIRATING TUBING
Applicant
Km Products
1349 W. Allegheny
Tucson,  AZ  85705
Applicant Contact ALAN R KENT
Correspondent
Km Products
1349 W. Allegheny
Tucson,  AZ  85705
Correspondent Contact ALAN R KENT
Regulation Number868.6810
Classification Product Code
BSY  
Date Received01/11/1985
Decision Date 03/21/1985
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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