FDA 510(k) Application Details - K833201

Device Classification Name Culture Media, Non-Selective And Differential

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510(K) Number K833201
Device Name Culture Media, Non-Selective And Differential
Applicant ACUMEDIA MANUFACTURERS, INC.

, US
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Regulation Number 866.2320

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Classification Product Code JSH
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Date Received 09/19/1983
Decision Date 10/27/1983
Decision SE - Substantially Equivalent
Classification Advisory Committee MI - Microbiology
Review Advisory Committee MI - Microbiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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