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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name i.v. start kit
510(k) Number K842898
Device Name CURITY I.V. START KIT
Applicant
THE KENDAL CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
THE KENDAL CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number880.5200
Classification Product Code
LRS  
Date Received07/23/1984
Decision Date 08/17/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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