Microprotein Reagent Set

FDA 510(k) K921412 · Sterling Diagnostics, Inc.

Substantially Equivalent

510(k) numberK921412

Submission

Device name
Microprotein Reagent Set
Applicant
Sterling Diagnostics, Inc.
Sterling Heights, MI, US
Received
March 24, 1992
Decision date
January 21, 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
CEK – Biuret (Colorimetric), Total Protein
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1635
Specialty
Clinical Chemistry

Other 510(k)s with product code CEK

510(k)DeviceApplicantDecision
K992846Hichem Total Protein ReagentCEK · Traditional Elan Holdings, Inc.10/18/1999SE
K973108Total Protein (Micro) Assay, Catalogue Number 450-50CEK · Traditional Diagnostic Chemicals , Ltd.03/02/1998SE
K980042Careside Total ProteinCEK · Traditional Exigent Diagnostics, Inc.02/04/1998SE
K971524Total Protein or TPCEK · Traditional Carolina Liquid Chemistries Corp.05/16/1997SE
K961864Csf/Urine Total ProteinCEK · Traditional Teco Diagnostics10/24/1996SE
K955905STC Diagnostics Auto-Lyte Urinary Protein AssayCEK · Traditional Solarcare Technologies Corp,Inc.05/30/1996SE
K955936Total Protein ReagentCEK · Traditional Derma Media Lab., Inc.03/12/1996SE
K950920Dupont Dimension Total Protein MethodCEK · Traditional Dupont Medical Products08/11/1995SE
K950234Total Protein Test (Tpro) Item Number: XXXXX/R1. R2CEK · Traditional Emd Chemicals, Inc.06/14/1995SE
K950128Total Protein Test (Tpro) Item XXXXX/R1. R2CEK · Traditional Emd Chemicals, Inc.05/15/1995SE

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Questions and answers

When was Microprotein Reagent Set cleared by the FDA?

Microprotein Reagent Set (K921412) received a 510(k) decision of Substantially Equivalent on January 21, 1993, 303 days after the submission was received.

What is the product code of K921412?

The FDA product code is CEK – Biuret (Colorimetric), Total Protein, a Class II (moderate risk) device regulated under 21 CFR 862.1635.