FDA 510(k) Applications for Medical Device Product Code: PZH ()

FDA 510(k) Applications for Medical Device Product Code "PZH"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K211115	Progenika Biopharma S.A., a Grifols company	A1AT Genotyping Test	05/13/2021
K171868	Progenika Biopharma S.A., a Grifols Company	A1AT Genotyping Test	11/11/2017
K192858	Progenika Biopharma S.A., A Grifols Company	A1AT Genotyping Test	11/05/2019