vWF Ag— 510(k) K220728
Substantially EquivalentSiemens Healthcare Diagnostics Products GmbH
FDA 510(k) clearance K220728 for vWF Ag, Substantially Equivalent on 2023-06-02. Applicant: Siemens Healthcare Diagnostics Products GmbH.
Clearance details
- Applicant
- Siemens Healthcare Diagnostics Products GmbH
- Product code
- Code GGP
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Marburg, DE
Data sourced from openFDA. This site is unofficial and independent of the FDA.