Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

T3 UPTAKE REAGENT SET

K-Number: K770845 · 1977-05-26

Decision Date1977-05-26
Product CodeKHQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

T3 UPTAKE REAGENT SET is the device name listed in this FDA 510(k) record. The listed applicant is The Dow Chemical Co.. It received FDA 510(k) clearance on 1977-05-26 under 510(k) number K770845. The device is classified under product code KHQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T3 UPTAKE REAGENT SET?

T3 UPTAKE REAGENT SET is a medical device that received FDA 510(k) clearance on 1977-05-26. The listed applicant is The Dow Chemical Co.. The 510(k) number is K770845.

When did T3 UPTAKE REAGENT SET receive FDA 510(k) clearance?

T3 UPTAKE REAGENT SET received FDA 510(k) clearance on 1977-05-26, under 510(k) number K770845.

Who is the listed applicant for T3 UPTAKE REAGENT SET?

The FDA 510(k) record lists The Dow Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for T3 UPTAKE REAGENT SET?

The FDA product code for T3 UPTAKE REAGENT SET is KHQ.

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.

Other records listing The Dow Chemical Co. 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.

View all 26 devices →

Related Devices (Code: KHQ)

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.

↑