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FDA 510(k)

HemosIL von Willebrand Factor Antigen

K-Number: K200033 · 2020-08-19

ApplicantInstrumentation Laboratory CO
Decision Date2020-08-19
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HemosIL von Willebrand Factor Antigen is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 2020-08-19 under 510(k) number K200033. 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 HemosIL von Willebrand Factor Antigen?

HemosIL von Willebrand Factor Antigen is a medical device that received FDA 510(k) clearance on 2020-08-19. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K200033.

When did HemosIL von Willebrand Factor Antigen receive FDA 510(k) clearance?

HemosIL von Willebrand Factor Antigen received FDA 510(k) clearance on 2020-08-19, under 510(k) number K200033.

Who is the listed applicant for HemosIL von Willebrand Factor Antigen?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HemosIL von Willebrand Factor Antigen?

The FDA product code for HemosIL von Willebrand Factor Antigen is GGP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT02628509Von Willebrand Factor As a Biological Sensor of Blood Flow in Percutaneous Cardiac ProcedureCOMPLETED

Other records listing Instrumentation Laboratory CO as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K233790ACL TOP 970 CLK230852HemosIL Chromogenic Factor IXK221359ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgMK223608GEM Premier 7000 with IQM3K223187HemosIL Liquid Anti-XaK231031ACL TOP Family 70 Series

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Related Devices (Code: GGP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251440CRYOcheck Chromogenic Factor VIIIPrecision Biologic, Inc.K230852HemosIL Chromogenic Factor IXInstrumentation Laboratory CompanyK220728vWF AgSiemens Healthcare Diagnostics Products GmbHK214002CRYOcheck Chromogenic Factor IXPrecision Biologic, Inc.K223402HemosIL von Willebrand Factor AntigenInstrumentation Laboratory COK193204Cryocheck Chromogenic Factor VIIIPrecision Biologic

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.

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