Dimension Total Triiodothyronine Calibrator (RC414)

FDA 510(k) K032697 · Dade Behring, Inc.

Substantially Equivalent

510(k) numberK032697

Submission

Device name
Dimension Total Triiodothyronine Calibrator (RC414)
Applicant
Dade Behring, Inc.
Newark, DE, US
Received
September 2, 2003
Decision date
November 7, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JIS – Calibrator, Primary
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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Questions and answers

When was Dimension Total Triiodothyronine Calibrator (RC414) cleared by the FDA?

Dimension Total Triiodothyronine Calibrator (RC414) (K032697) received a 510(k) decision of Substantially Equivalent on November 7, 2003, 66 days after the submission was received.

What is the product code of K032697?

The FDA product code is JIS – Calibrator, Primary, a Class II (moderate risk) device regulated under 21 CFR 862.1150.