FDA 510(k)

ABBOTT TDX TOTAL T3 PLUS

K-Number: K894238 · 1989-10-31

Decision Date1989-10-31

Product CodeCDP

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

ABBOTT TDX TOTAL T3 PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1989-10-31 under 510(k) number K894238. 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 ABBOTT TDX TOTAL T3 PLUS?

ABBOTT TDX TOTAL T3 PLUS is a medical device that received FDA 510(k) clearance on 1989-10-31. The listed applicant is Abbott Laboratories. The 510(k) number is K894238.

When did ABBOTT TDX TOTAL T3 PLUS receive FDA 510(k) clearance?

ABBOTT TDX TOTAL T3 PLUS received FDA 510(k) clearance on 1989-10-31, under 510(k) number K894238.

Who is the listed applicant for ABBOTT TDX TOTAL T3 PLUS?

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 ABBOTT TDX TOTAL T3 PLUS?

The FDA product code for ABBOTT TDX TOTAL T3 PLUS is CDP.

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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.