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FDA 510(k)

VIRGO BETA 2 GLYCOPROTEIN IGG ANTIBODY KIT

K-Number: K992224 · 1999-08-30

Decision Date1999-08-30
Product CodeMSV
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

VIRGO BETA 2 GLYCOPROTEIN IGG ANTIBODY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Hemagen Diagnostics, Inc.. It received FDA 510(k) clearance on 1999-08-30 under 510(k) number K992224. The device is classified under product code MSV. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIRGO BETA 2 GLYCOPROTEIN IGG ANTIBODY KIT?

VIRGO BETA 2 GLYCOPROTEIN IGG ANTIBODY KIT is a medical device that received FDA 510(k) clearance on 1999-08-30. The listed applicant is Hemagen Diagnostics, Inc.. The 510(k) number is K992224.

When did VIRGO BETA 2 GLYCOPROTEIN IGG ANTIBODY KIT receive FDA 510(k) clearance?

VIRGO BETA 2 GLYCOPROTEIN IGG ANTIBODY KIT received FDA 510(k) clearance on 1999-08-30, under 510(k) number K992224.

Who is the listed applicant for VIRGO BETA 2 GLYCOPROTEIN IGG ANTIBODY KIT?

The FDA 510(k) record lists Hemagen Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIRGO BETA 2 GLYCOPROTEIN IGG ANTIBODY KIT?

The FDA product code for VIRGO BETA 2 GLYCOPROTEIN IGG ANTIBODY KIT is MSV.

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.

Other records listing Hemagen Diagnostics, Inc. 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.

View all 52 devices →

Related Devices (Code: MSV)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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