FDA 510(k) Applications Submitted by Christine Perkins

FDA 510(k) Number	Submission Date	Device Name	Applicant
K190879	04/04/2019	N Latex FLC kappa, N Latex FLC lambda	Siemens Healthcare Diagnostics Products GmbH
K171072	04/10/2017	N Latex Cystatin C; N Protein Standard UY	Siemens Healthcare Diagnostics Products GmbH
K201496	06/05/2020	N Latex FLC kappa, N Latex FLC lambda	Siemens Healthcare Diagnostics Products GmbH
K171742	06/12/2017	N Latex FLC kappa assay, N Latex FLC Lambda assay, N FLC Standard SL, N FLC Control SL1 & SL2	Siemens Healthcare Diagnostics Products GmbH
K182098	08/03/2018	N Latex FLC kappa assay, N Latex FLC lambda assay	Siemens Healthcare Diagnostics Products GmbH
K193047	11/01/2019	N Latex FLC kappa, N Latex FLC lambda	Siemens Healthcare Diagnostics Products GmbH