Last synced on 9 May 2025 at 11:05 pm

N Latex FLC kappa assay, N Latex FLC Lambda assay, N FLC Standard SL, N FLC Control SL1 & SL2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171742
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics Products GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/17/2017
Days to Decision
158 days
Submission Type
Summary

N Latex FLC kappa assay, N Latex FLC Lambda assay, N FLC Standard SL, N FLC Control SL1 & SL2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171742
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics Products GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/17/2017
Days to Decision
158 days
Submission Type
Summary