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FDA 510(k)

LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY

K-Number: K914835 · 1991-12-17

Decision Date1991-12-17
Product CodeCEC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is London Diagnostics, Inc.. It received FDA 510(k) clearance on 1991-12-17 under 510(k) number K914835. 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 LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY?

LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY is a medical device that received FDA 510(k) clearance on 1991-12-17. The listed applicant is London Diagnostics, Inc.. The 510(k) number is K914835.

When did LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY receive FDA 510(k) clearance?

LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY received FDA 510(k) clearance on 1991-12-17, under 510(k) number K914835.

Who is the listed applicant for LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY?

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

What is the FDA product code for LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY?

The FDA product code for LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY is CEC.

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 London Diagnostics, 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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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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