FDA 510(k) Application Details - K837322

Device Classification Name

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510(K) Number K837322
Device Name NOVO CEREBROGRAPH
Applicant NOVO DIAGNOSTIC SYSTEMS


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Regulation Number

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Classification Product Code
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Date Received 03/24/1983
Decision Date 04/21/1983
Decision SE - Substantially Equivalent
Classification Advisory Committee RA - Radiology
Review Advisory Committee -
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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