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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Kit, Identification, Glucose Nonfermenter
510(k) Number K770745
Device Name PANEL, GNF, MICRO-ID
Applicant
Micro-Media Systems, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Micro-Media Systems, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.2660
Classification Product Code
JSW  
Date Received04/22/1977
Decision Date 06/23/1977
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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