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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
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