Serum Iron Reagent Set

FDA 510(k) K812840 · Anco Medical Reagents & Assoc.

Substantially Equivalent

510(k) numberK812840

Submission

Device name
Serum Iron Reagent Set
Applicant
Anco Medical Reagents & Assoc.
Mchenry, IL, US
Received
October 9, 1981
Decision date
December 3, 1981
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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K051115Sentinel Iron LiquidJIY · Traditional Sentinel Ch. Srl08/25/2005SE
K033983Vitalab Iron ReagentJIY · Traditional Clinical Data, Inc.05/21/2004SE
K030528Atac Iron Reagent, Atac Tibc Column Kit and Iron Calibrator (500 Ug/Dl)JIY · Traditional Clinical Data06/17/2003SE
K020816Iron-Pc-Sl Assay Model # 151-10, 151-26JIY · Traditional Diagnostic Chemicals , Ltd.05/14/2002SE
K013097Wiener Lab.Fer-Color Aa, Model 5X 20 ML Cat.N 1492003JIY · Traditional Wiener Laboratories Saic11/13/2001SE
K981241IronJIY · Traditional Abbott Laboratories05/01/1998SE
K973933Serum Iron-Sl Assay, Catalogue Numbers 157-10, 157-30JIY · Traditional Diagnostic Chemicals , Ltd.11/04/1997SE
K972363Il Test IronJIY · Traditional Instrumentation Laboratory CO08/15/1997SE

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K820491SGPT Reagent SetCKD · Traditional 03/11/1982SE
K820466Sgot Reagent SetCIQ · Traditional 03/11/1982SE
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Questions and answers

When was Serum Iron Reagent Set cleared by the FDA?

Serum Iron Reagent Set (K812840) received a 510(k) decision of Substantially Equivalent on December 3, 1981, 55 days after the submission was received.

What is the product code of K812840?

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