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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Atomic Absorption Spectrophotometer, General Use
510(k) Number K780390
Device Name SPECTROPHOTOMETER, ABSORPTION, ATOMIC
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 Number862.2850
Classification Product Code
JXR  
Date Received03/10/1978
Decision Date 03/22/1978
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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