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FDA 510(k)

VIRATEST-DIA(TM) MEASLES (RUBEOLA)

K-Number: K910290 · 1992-03-18

Decision Date1992-03-18
Product CodeLJB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VIRATEST-DIA(TM) MEASLES (RUBEOLA) is the device name listed in this FDA 510(k) record. The listed applicant is Virus Reference Laboratory, Inc.. It received FDA 510(k) clearance on 1992-03-18 under 510(k) number K910290. The device is classified under product code LJB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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

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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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