NDS Thyroxine Test Kit & NDS Thyroxine Calibrator

FDA 510(k) K897072 · Kallestad Diag, A Div. of Erbamont, Inc.

Substantially Equivalent

510(k) numberK897072

Submission

Device name
NDS Thyroxine Test Kit & NDS Thyroxine Calibrator
Applicant
Kallestad Diag, A Div. of Erbamont, Inc.
Chaska, MN, US
Received
December 22, 1989
Decision date
March 29, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KLI – Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1700
Specialty
Clinical Chemistry

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Questions and answers

When was NDS Thyroxine Test Kit & NDS Thyroxine Calibrator cleared by the FDA?

NDS Thyroxine Test Kit & NDS Thyroxine Calibrator (K897072) received a 510(k) decision of Substantially Equivalent on March 29, 1990, 97 days after the submission was received.

What is the product code of K897072?

The FDA product code is KLI – Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine, a Class II (moderate risk) device regulated under 21 CFR 862.1700.