Atellica IM Ferritin Assay— 510(k) K171642

Substantially Equivalent

Siemens Healthcare Diagnostics, Inc.

FDA 510(k) clearance K171642 for Atellica IM Ferritin Assay, Substantially Equivalent on 2017-08-31. Applicant: Siemens Healthcare Diagnostics, Inc..

Clearance details

Applicant: Siemens Healthcare Diagnostics, Inc.
Product code: Code DBF
Advisory panel: Immunology
Date received: 2017-06-02
Decision date: 2017-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarrytown, NY, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.