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)

FREE T4 RIA TEST SET

K-Number: K813465 · 1981-12-31

Decision Date1981-12-31
Product CodeCEC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FREE T4 RIA TEST SET is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex Laboratories, Inc.. It received FDA 510(k) clearance on 1981-12-31 under 510(k) number K813465. The device is classified under product code CEC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREE T4 RIA TEST SET?

FREE T4 RIA TEST SET is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K813465.

When did FREE T4 RIA TEST SET receive FDA 510(k) clearance?

FREE T4 RIA TEST SET received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813465.

Who is the listed applicant for FREE T4 RIA TEST SET?

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

What is the FDA product code for FREE T4 RIA TEST SET?

The FDA product code for FREE T4 RIA TEST SET is CEC.

Other records listing Ventrex Laboratories, 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.

View all 82 devices →

Related Devices (Code: CEC)

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.

↑