FDA 510(k) Applications Submitted by Asuragen, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
DEN190023 04/18/2019 AmplideX Fragile X Dx & Carrier Screen Kit Asuragen, Inc.
DEN160003 01/19/2016 Quantidex qPCR BCR-ABL IS Kit ASURAGEN, INC.
K113420 11/18/2011 RNARETAIN ASURAGEN, INC.


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