King Diagnostics Iron and Total Iron Binding Capacity Reagent

FDA 510(k) K933329 · King Diagnostics, Inc.

Substantially Equivalent

510(k) numberK933329

Submission

Device name
King Diagnostics Iron and Total Iron Binding Capacity Reagent
Applicant
King Diagnostics, Inc.
Indianapolis, IN, US
Received
July 8, 1993
Decision date
October 22, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JMO – Ferrozine (Colorimetric) Iron Binding Capacity
Device class
Class I (low risk)
Regulation
21 CFR 862.1415
Specialty
Clinical Chemistry

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K013102Wiener Lab. Fer-Color Transferrina, Model Aux. Reagents for 25 Samples Cat. 1492002JMO · Traditional Wiener Laboratories Saic11/13/2001SE
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Questions and answers

When was King Diagnostics Iron and Total Iron Binding Capacity Reagent cleared by the FDA?

King Diagnostics Iron and Total Iron Binding Capacity Reagent (K933329) received a 510(k) decision of Substantially Equivalent on October 22, 1993, 106 days after the submission was received.

What is the product code of K933329?

The FDA product code is JMO – Ferrozine (Colorimetric) Iron Binding Capacity, a Class I (low risk) device regulated under 21 CFR 862.1415.