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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Plasminogen, Antigen, Antiserum, Control
510(k) Number K811777
Device Name HELENA PLASMINOGEN QUIPLATE PROCEDURE
Applicant
Helena Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Helena Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.5715
Classification Product Code
DDX  
Date Received06/23/1981
Decision Date 07/02/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Immunology
510k Review Panel Immunology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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