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FDA 510(k)

MEASLES VIRUS RUBEOLA

K-Number: K843662 · 1985-09-26

ApplicantInstitute Virion , Ltd.
Decision Date1985-09-26
Product CodeGRJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MEASLES VIRUS RUBEOLA is the device name listed in this FDA 510(k) record. The listed applicant is Institute Virion , Ltd.. It received FDA 510(k) clearance on 1985-09-26 under 510(k) number K843662. The device is classified under product code GRJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEASLES VIRUS RUBEOLA?

MEASLES VIRUS RUBEOLA is a medical device that received FDA 510(k) clearance on 1985-09-26. The listed applicant is Institute Virion , Ltd.. The 510(k) number is K843662.

When did MEASLES VIRUS RUBEOLA receive FDA 510(k) clearance?

MEASLES VIRUS RUBEOLA received FDA 510(k) clearance on 1985-09-26, under 510(k) number K843662.

Who is the listed applicant for MEASLES VIRUS RUBEOLA?

The FDA 510(k) record lists Institute Virion , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEASLES VIRUS RUBEOLA?

The FDA product code for MEASLES VIRUS RUBEOLA is GRJ.

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Other records listing Institute Virion , Ltd. 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.

K862814COMPLEMENT-FIXATION TEST FOR CAMPYLOBACTER JEJUNIK843673RESPIRATORY SYNCYTIAL VIRUSK843660IN FLUENZA B VIRUSK843657CYTOMEGALOVIRUSK843658H. SIMPLEX VIRUSK843667PARAINFLUENZA 3

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Related Devices (Code: GRJ)

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.

K802932MEASLES VIRUS & CONTROLSOrion Diagnostica, Inc.

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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