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FDA 510(k)

FREE T4 IMMUNOASSAY KIT

K-Number: K900060 · 1990-03-29

Decision Date1990-03-29
Product CodeCEC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FREE T4 IMMUNOASSAY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Magnetics, Inc.. It received FDA 510(k) clearance on 1990-03-29 under 510(k) number K900060. 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 IMMUNOASSAY KIT?

FREE T4 IMMUNOASSAY KIT is a medical device that received FDA 510(k) clearance on 1990-03-29. The listed applicant is Advanced Magnetics, Inc.. The 510(k) number is K900060.

When did FREE T4 IMMUNOASSAY KIT receive FDA 510(k) clearance?

FREE T4 IMMUNOASSAY KIT received FDA 510(k) clearance on 1990-03-29, under 510(k) number K900060.

Who is the listed applicant for FREE T4 IMMUNOASSAY KIT?

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

What is the FDA product code for FREE T4 IMMUNOASSAY KIT?

The FDA product code for FREE T4 IMMUNOASSAY KIT 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 Advanced Magnetics, 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.

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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