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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Susceptibility Test Discs, Antimicrobial
510(k) Number K812993
Device Name MOXALACTOM 30MCG ANTIMICROBIAL SUS. DISK
Applicant
General Diagnostics
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
General Diagnostics
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.1620
Classification Product Code
JTN  
Date Received10/26/1981
Decision Date 11/10/1981
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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