FDA 510(k), K101454, MAMMAPRINT

FDA 510(k), K101454, MAMMAPRINT

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510(K) Number: K101454
Device Name: MAMMAPRINT
Manufacturer:
Device Classification Name: Classifier, Prognostic, Recurrence Risk Assessment, Rna Gene Expression, Breast Cancer
Regulation Number: 866.6040
Classification Product Code: NYI
Date Received: 05/25/2010
Decision Date: 01/28/2011
Regulation Medical Specialty: Immunology
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