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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
510(k) Number K831747
Device Name PLASMA THERAPY TUBESET-E100 SERIES
Applicant
Parker Hannifin Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Parker Hannifin Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number876.5820
Classification Product Code
FJK  
Date Received06/01/1983
Decision Date 06/30/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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