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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 K892441
Device Name KENDALL CURITY SUCTION CATHETERS
Applicant
The Kendal Co.
One Federal St.
Boston,  MA  02110
Applicant Contact WILLIAM D CURTIN
Correspondent
The Kendal Co.
One Federal St.
Boston,  MA  02110
Correspondent Contact WILLIAM D CURTIN
Regulation Number868.6810
Classification Product Code
BSY  
Date Received04/10/1989
Decision Date 05/31/1989
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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