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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Coated Tube Sep.
510(k) Number K791355
Device Name VENTRE/SEP DIGOXIN RADIOIMMUNOASSAY KIT
Applicant
Ventrex Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Ventrex Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number862.3320
Classification Product Code
DPO  
Date Received07/21/1979
Decision Date 08/10/1979
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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