Coulter Serum Iron/Uibc Reagent

FDA 510(k) K902173 · Coulter Corp.

Substantially Equivalent

510(k) numberK902173

Submission

Device name
Coulter Serum Iron/Uibc Reagent
Applicant
Coulter Corp.
Hialeah, FL, US
Received
May 14, 1990
Decision date
June 12, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JIY – Photometric Method, Iron (Non-Heme)
Device class
Class I (low risk)
Regulation
21 CFR 862.1410
Specialty
Clinical Chemistry

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Questions and answers

When was Coulter Serum Iron/Uibc Reagent cleared by the FDA?

Coulter Serum Iron/Uibc Reagent (K902173) received a 510(k) decision of Substantially Equivalent on June 12, 1990, 29 days after the submission was received.

What is the product code of K902173?

The FDA product code is JIY – Photometric Method, Iron (Non-Heme), a Class I (low risk) device regulated under 21 CFR 862.1410.