Serum Iron/Vibc Reagent Set

FDA 510(k) K852161 · Livonia Diagnostics, Inc.

Substantially Equivalent

510(k) numberK852161

Submission

Device name
Serum Iron/Vibc Reagent Set
Applicant
Livonia Diagnostics, Inc.
Livonia, MI, US
Received
May 20, 1985
Decision date
June 10, 1985
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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Questions and answers

When was Serum Iron/Vibc Reagent Set cleared by the FDA?

Serum Iron/Vibc Reagent Set (K852161) received a 510(k) decision of Substantially Equivalent on June 10, 1985, 21 days after the submission was received.

What is the product code of K852161?

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