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BioPorto Receives FDA 510(k) Clearance for NGAL Test in the United States First Test to Aid in Assessing AKI Risk for Patients Aged 3 Months Through 21 Years -December 07, 2023 at 04:23 pm EST

December 7, 2023 Announcement no. 20 BioPorto Receives FDA 510 Clearance for NGAL Test in the United StatesFirst Test to Aid in Assessing AKI Risk for Patients Aged 3 Months Through 21 Years ...
United States Ashleyr Robinson Prasad Devarajan Global Press Relations Drug Administration Bioporto Company Announcements

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