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FDA 510(k)

OREIA-TU THYROID UPTAKER RATIO ASSAY

K-Number: K791172 · 1979-10-30

ApplicantOrganon, Inc.
Decision Date1979-10-30
Product Code
DecisionSubstantially Equivalent

Device Summary

OREIA-TU THYROID UPTAKER RATIO ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Organon, Inc.. It received FDA 510(k) clearance on 1979-10-30 under 510(k) number K791172. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OREIA-TU THYROID UPTAKER RATIO ASSAY?

OREIA-TU THYROID UPTAKER RATIO ASSAY is a medical device that received FDA 510(k) clearance on 1979-10-30. The listed applicant is Organon, Inc.. The 510(k) number is K791172.

When did OREIA-TU THYROID UPTAKER RATIO ASSAY receive FDA 510(k) clearance?

OREIA-TU THYROID UPTAKER RATIO ASSAY received FDA 510(k) clearance on 1979-10-30, under 510(k) number K791172.

Who is the listed applicant for OREIA-TU THYROID UPTAKER RATIO ASSAY?

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

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Other records listing Organon, Inc. 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.

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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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