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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Thin Layer Chromatography, Barbiturate
510(k) Number K800364
Device Name ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202
Applicant
Hoffrel Instruments, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Hoffrel Instruments, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number862.3150
Classification Product Code
DKX  
Date Received02/20/1980
Decision Date 03/12/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Toxicology
510k Review Panel Toxicology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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