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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls
510(k) Number K900072
Device Name IMMUNODOT AUTOIMMUNITY SCREENING PANEL 2
Applicant
General Biometrics, Inc.
15222 Ave. Of Science
Suite A
San Diego,  CA  92128
Applicant Contact BRYAN L KIEHL
Correspondent
General Biometrics, Inc.
15222 Ave. Of Science
Suite A
San Diego,  CA  92128
Correspondent Contact BRYAN L KIEHL
Regulation Number866.5100
Classification Product Code
LJM  
Date Received01/05/1990
Decision Date 01/24/1990
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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