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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 K833633
Device Name BRONCHITRAC DF DUAL RESP/CATHETER
Applicant
ACKRAD LABORATORIES
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
ACKRAD LABORATORIES
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.6810
Classification Product Code
BSY  
Date Received10/17/1983
Decision Date 12/08/1983
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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