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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Culture Media, Non-Selective And Non-Differential
510(k) Number K873257
Device Name GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.
Applicant
Central Media
10386 Rockingham Dr.
Sacramento,  CA  95827
Applicant Contact REBECCA CLARK
Correspondent
Central Media
10386 Rockingham Dr.
Sacramento,  CA  95827
Correspondent Contact REBECCA CLARK
Regulation Number866.2300
Classification Product Code
JSG  
Date Received08/11/1987
Decision Date 11/06/1987
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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