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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stopcock, I.V. Set
510(k) Number K842173
Device Name DISPOSABLE STOPCOCKS
Applicant
PROCEDURE PRODUCTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
PROCEDURE PRODUCTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number880.5440
Classification Product Code
FMG  
Date Received05/15/1984
Decision Date 09/05/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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