INNOVANCE VWF Ac— 510(k) DEN200067

Unknown

Siemens Healthcare Diagnostics Products GmbH

FDA 510(k) clearance DEN200067 for INNOVANCE VWF Ac, Unknown on 2022-09-29. Applicant: Siemens Healthcare Diagnostics Products GmbH. Device class: 2.

Clearance details

Applicant: Siemens Healthcare Diagnostics Products GmbH
Product code: Code QTY
Device class: Class 2
Regulation: 21 CFR 864.7293
Advisory panel: Hematology
Date received: 2020-10-28
Decision date: 2022-09-29
Decision: Unknown
Clearance type: Direct
Location: Marburg, DE

View on FDA.gov ↗

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