Chem 1 Clinical Analyzer (Method Urine Creatinine)

FDA 510(k) K901229 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK901229

Submission

Device name
Chem 1 Clinical Analyzer (Method Urine Creatinine)
Applicant
Technicon Instruments Corp.
Tarrytown, NY, US
Received
March 14, 1990
Decision date
May 4, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CGX – Alkaline Picrate, Colorimetry, Creatinine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1225
Specialty
Clinical Chemistry

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K161494Atellica CH Creatinine_2 (Crea_2), Atellica CH Chemistry Calibrator (CHEM CAL)CGX · Traditional Siemens Healthcare Diagnostics, Inc.11/15/2016SE
K132638Dimension Creatinine (CRE2) Flex Reagent CartridgeCGX · Traditional Siemens Healthcare Diagnostics, Inc.01/27/2014SE
K133728Dimension Vista Creatinine (CRE2) Flex Reagent CartridgeCGX · Traditional Siemens Healthcare Diagnostics, Inc.01/24/2014SE
K123586Easyra Creatinine ReagentCGX · Special Medica Corporation05/15/2013SE
K110530Abx Pentra Creatinine 120 CP; Abx Pentra Multical; Abx Pentra N Control; Abx Pentra P…CGX · Abbreviated Horiba Abx SAS04/30/2012SE

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Questions and answers

When was Chem 1 Clinical Analyzer (Method Urine Creatinine) cleared by the FDA?

Chem 1 Clinical Analyzer (Method Urine Creatinine) (K901229) received a 510(k) decision of Substantially Equivalent on May 4, 1990, 51 days after the submission was received.

What is the product code of K901229?

The FDA product code is CGX – Alkaline Picrate, Colorimetry, Creatinine, a Class II (moderate risk) device regulated under 21 CFR 862.1225.