HERPES VIRUS AGGLUTINATION TEST
K-Number: K842887 · 1985-02-26
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Device Summary
Frequently Asked Questions
What is the HERPES VIRUS AGGLUTINATION TEST?
HERPES VIRUS AGGLUTINATION TEST is a medical device that received FDA 510(k) clearance on 1985-02-26. The listed applicant is Scientific Research. The 510(k) number is K842887.
When did HERPES VIRUS AGGLUTINATION TEST receive FDA 510(k) clearance?
HERPES VIRUS AGGLUTINATION TEST received FDA 510(k) clearance on 1985-02-26, under 510(k) number K842887.
Who is the listed applicant for HERPES VIRUS AGGLUTINATION TEST?
The FDA 510(k) record lists Scientific Research as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HERPES VIRUS AGGLUTINATION TEST?
The FDA product code for HERPES VIRUS AGGLUTINATION TEST is GQO.
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 Scientific Research 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: GQO)
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.
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