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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Chromatography (Liquid, Gel), Clinical Use
510(k) Number K841890
Device Name VARIAN 2000 LIQUID CHROMATOGRAPHY ANALY
Applicant
Varian Assoc., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Varian Assoc., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number862.2260
Classification Product Code
KZR  
Date Received05/07/1984
Decision Date 06/14/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Toxicology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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