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FDA 510(k)

Q-FEVER

K-Number: K843672 · 1985-08-08

ApplicantInstitute Virion , Ltd.
Decision Date1985-08-08
Product CodeGPS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

Q-FEVER 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 1985-08-08 under 510(k) number K843672. The device is classified under product code GPS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q-FEVER?

Q-FEVER is a medical device that received FDA 510(k) clearance on 1985-08-08. The listed applicant is Institute Virion , Ltd.. The 510(k) number is K843672.

When did Q-FEVER receive FDA 510(k) clearance?

Q-FEVER received FDA 510(k) clearance on 1985-08-08, under 510(k) number K843672.

Who is the listed applicant for Q-FEVER?

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 Q-FEVER?

The FDA product code for Q-FEVER is GPS.

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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 JEJUNIK843662MEASLES VIRUS RUBEOLAK843660IN FLUENZA B VIRUSK843657CYTOMEGALOVIRUSK843658H. SIMPLEX VIRUSK843673RESPIRATORY SYNCYTIAL VIRUS

View all 16 devices →

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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