vWF Ag— 510(k) K220728

Name: FDA 510(k) clearance K220728
Creator: U.S. Food and Drug Administration
Published: 2023-06-02

Substantially Equivalent

Siemens Healthcare Diagnostics Products GmbH

FDA 510(k) clearance K220728 for vWF Ag, Substantially Equivalent on 2023-06-02. Applicant: Siemens Healthcare Diagnostics Products GmbH. Device class: 2.

Clearance details

Applicant: Siemens Healthcare Diagnostics Products GmbH
Product code: Code GGP
Device class: Class 2
Regulation: 21 CFR 864.7290
Advisory panel: Hematology
Date received: 2022-03-14
Decision date: 2023-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marburg, DE

Download summary PDF View on FDA.gov ↗

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