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FDA 510(k)

VZV ANTIGEN CONTROL SLIDES

K-Number: K964872 · 1997-03-18

Decision Date1997-03-18
Product CodeGQW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VZV ANTIGEN CONTROL SLIDES is the device name listed in this FDA 510(k) record. The listed applicant is Viral Antigens, Inc.. It received FDA 510(k) clearance on 1997-03-18 under 510(k) number K964872. The device is classified under product code GQW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VZV ANTIGEN CONTROL SLIDES?

VZV ANTIGEN CONTROL SLIDES is a medical device that received FDA 510(k) clearance on 1997-03-18. The listed applicant is Viral Antigens, Inc.. The 510(k) number is K964872.

When did VZV ANTIGEN CONTROL SLIDES receive FDA 510(k) clearance?

VZV ANTIGEN CONTROL SLIDES received FDA 510(k) clearance on 1997-03-18, under 510(k) number K964872.

Who is the listed applicant for VZV ANTIGEN CONTROL SLIDES?

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

What is the FDA product code for VZV ANTIGEN CONTROL SLIDES?

The FDA product code for VZV ANTIGEN CONTROL SLIDES is GQW.

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 Viral Antigens, 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: GQW)

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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