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FDA 510(k)

IMX FREE TRIIODOTHYRONINE

K-Number: K905261 · 1991-01-23

ApplicantAbbott Laboratories
Decision Date1991-01-23
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IMX FREE TRIIODOTHYRONINE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1991-01-23 under 510(k) number K905261. The device is classified under product code CDP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMX FREE TRIIODOTHYRONINE?

IMX FREE TRIIODOTHYRONINE is a medical device that received FDA 510(k) clearance on 1991-01-23. The listed applicant is Abbott Laboratories. The 510(k) number is K905261.

When did IMX FREE TRIIODOTHYRONINE receive FDA 510(k) clearance?

IMX FREE TRIIODOTHYRONINE received FDA 510(k) clearance on 1991-01-23, under 510(k) number K905261.

Who is the listed applicant for IMX FREE TRIIODOTHYRONINE?

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

What is the FDA product code for IMX FREE TRIIODOTHYRONINE?

The FDA product code for IMX FREE TRIIODOTHYRONINE is CDP.

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Related Devices (Code: CDP)

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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