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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Igd, Rhodamine, Antigen, Antiserum, Control
510(k) Number K915838
Device Name OPUS FERRITIN TEST SYSTEM
Applicant
Pb Diagnostic Systems, Inc.
151 University Ave.
Westwood,  MA  02090
Applicant Contact LORI BARANAUSKAS
Correspondent
Pb Diagnostic Systems, Inc.
151 University Ave.
Westwood,  MA  02090
Correspondent Contact LORI BARANAUSKAS
Regulation Number866.5510
Classification Product Code
DGE  
Date Received12/24/1991
Decision Date 03/18/1992
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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