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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Antisera, Fluorescent, All Types, Hemophilus Spp.
510(k) Number K834067
Device Name LEGIONELLA DIFFERENTIATION DISK
Applicant
Remel Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Remel Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.3300
Classification Product Code
GRO  
Date Received11/25/1983
Decision Date 01/03/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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