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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pneumocystis Carinii
510(k) Number K904400
Device Name MERIFLUOR TM PNEUMOCYSTIS MODIFICATION
Applicant
Meridian Diagnostics, Inc.
3471 River Hills Dr.
Cincinnati,  OH  45244
Applicant Contact ALLEN NICKOL
Correspondent
Meridian Diagnostics, Inc.
3471 River Hills Dr.
Cincinnati,  OH  45244
Correspondent Contact ALLEN NICKOL
Regulation Number866.3780
Classification Product Code
LYF  
Date Received09/21/1990
Decision Date 10/16/1990
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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