VIRGO B2 GLYCOPROTEIN I IGA ANTIBODY KIT
K-Number: K992241 · 1999-08-30
Advertisement
Device Summary
Frequently Asked Questions
What is the VIRGO B2 GLYCOPROTEIN I IGA ANTIBODY KIT?
VIRGO B2 GLYCOPROTEIN I IGA 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 K992241.
When did VIRGO B2 GLYCOPROTEIN I IGA ANTIBODY KIT receive FDA 510(k) clearance?
VIRGO B2 GLYCOPROTEIN I IGA ANTIBODY KIT received FDA 510(k) clearance on 1999-08-30, under 510(k) number K992241.
Who is the listed applicant for VIRGO B2 GLYCOPROTEIN I IGA 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 B2 GLYCOPROTEIN I IGA ANTIBODY KIT?
The FDA product code for VIRGO B2 GLYCOPROTEIN I IGA 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement