FDA 510(k) Application Details - K850522

Device Classification Name Media And Components, Synthetic Cell And Tissue Culture

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510(K) Number K850522
Device Name Media And Components, Synthetic Cell And Tissue Culture
Applicant MEDIATECH, INC.
EDWARD J. MILLER
1090 VERMONT AVE., NW #1200
WASHINGTON, DC US
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Contact HARGRAVE, DEV
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Regulation Number 864.2220

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Classification Product Code KIT
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Date Received 02/08/1985
Decision Date 02/27/1985
Decision SE - Substantially Equivalent
Classification Advisory Committee MI - Microbiology
Review Advisory Committee HE - Hematology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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