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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Igd, Antigen, Antiserum, Control
510(k) Number K872834
Device Name TITAN GEL IFE ANTISERUM TO IGD-9409 & IGE-9410
Applicant
Helena Laboratories
1530 Lindbergh Dr.
P.O. Box 752
Beaumont,  TX  77704
Applicant Contact PAT FRANKS
Correspondent
Helena Laboratories
1530 Lindbergh Dr.
P.O. Box 752
Beaumont,  TX  77704
Correspondent Contact PAT FRANKS
Regulation Number866.5510
Classification Product Code
CZJ  
Date Received07/17/1987
Decision Date 08/12/1987
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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