VIRATEST-DIA(TM) MEASLES (RUBEOLA)
K-Number: K910290 · 1992-03-18
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Device Summary
Frequently Asked Questions
What is the VIRATEST-DIA(TM) MEASLES (RUBEOLA)?
VIRATEST-DIA(TM) MEASLES (RUBEOLA) is a medical device that received FDA 510(k) clearance on 1992-03-18. The listed applicant is Virus Reference Laboratory, Inc.. The 510(k) number is K910290.
When did VIRATEST-DIA(TM) MEASLES (RUBEOLA) receive FDA 510(k) clearance?
VIRATEST-DIA(TM) MEASLES (RUBEOLA) received FDA 510(k) clearance on 1992-03-18, under 510(k) number K910290.
Who is the listed applicant for VIRATEST-DIA(TM) MEASLES (RUBEOLA)?
The FDA 510(k) record lists Virus Reference Laboratory, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIRATEST-DIA(TM) MEASLES (RUBEOLA)?
The FDA product code for VIRATEST-DIA(TM) MEASLES (RUBEOLA) is LJB.
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.
Related Devices (Code: LJB)
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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