vWF Ag
K-Number: K220728 · 2023-06-02
Decision Date2023-06-02
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent
Device Summary
vWF Ag is a medical device manufactured by Siemens Healthcare Diagnostics Products GmbH. It received FDA 510(k) clearance on 2023-06-02 under approval number K220728. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the vWF Ag?
vWF Ag is a medical device that received FDA 510(k) clearance on 2023-06-02. It is manufactured by Siemens Healthcare Diagnostics Products GmbH. The 510(k) number is K220728.
When was vWF Ag approved by the FDA?
vWF Ag received FDA 510(k) clearance on 2023-06-02, under approval number K220728.
What company makes vWF Ag?
vWF Ag is manufactured by Siemens Healthcare Diagnostics Products GmbH.
What is the FDA product code for vWF Ag?
The FDA product code for vWF Ag is GGP.
Other Devices by Siemens Healthcare Diagnostics Products GmbH
K162688Sysmex CS-2100i
K162420Sysmex Automated Blood Coagulation Analyzer CS-5100
K161317Sysmex Automated Blood Coagulation Analyzer CS-5100
K161312Sysmex Automated Blood Coagulation Analyzer CS-2100i
K151259Sysmex Automated Blood Coagulation Analyzer CS-2100i
K171742N Latex FLC kappa assay, N Latex FLC Lambda assay, N FLC Standard SL, N FLC Control SL1 & SL2
Related Devices (Code: GGP)
K181525INNOVANCE Free PS AgSiemens Healthcare Diagnostics Products GmbH
K183440CRYOcheck FVIII Inhibitor KitPrecision Biologic, Inc.
K200033HemosIL von Willebrand Factor AntigenInstrumentation Laboratory CO
K193204Cryocheck Chromogenic Factor VIIIPrecision Biologic
K214002CRYOcheck Chromogenic Factor IXPrecision Biologic, Inc.
K223402HemosIL von Willebrand Factor AntigenInstrumentation Laboratory CO
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.