Reagents Serum Creatine Using Techicon

FDA 510(k) K802156 · Panmed, Inc.

Substantially Equivalent

510(k) numberK802156

Submission

Device name
Reagents Serum Creatine Using Techicon
Applicant
Panmed, Inc.
Mchenry, IL, US
Received
September 8, 1980
Decision date
October 10, 1980
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
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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

More from Horiba Abx SAS

510(k)DeviceDecision
K852767Erythocyte CreatineJLA · Traditional 11/13/1986SE
K820642Sickle-CheckGHM · Traditional 04/14/1982SE
K8021648-HYDROXYQUINOLINE, Cresolphthalein Com.CIC · Traditional 10/10/1980SE
K802163Chloride Color & Chloride Sample DiluentCHJ · Traditional 10/10/1980SE
K802162CO2 Color Reagent & CO2 Sample DiluentKMS · Traditional 10/10/1980SE
K802161Biuret Reagent & Total Protein Blank SolCEK · Traditional 10/10/1980SE
K802160Bun Color Reagent & Bun Acid UsedCDW · Traditional 10/10/1980SE
K802159Ammonium Molybdate Inorganic PhosphorusCEO · Traditional 10/10/1980SE
K802158Postassium Buffer Sol. & Wash SolutionCEM · Traditional 10/10/1980SE
K802157BCG Reagent Serum Albumin W/TechniconCIX · Traditional 10/10/1980SE

Questions and answers

When was Reagents Serum Creatine Using Techicon cleared by the FDA?

Reagents Serum Creatine Using Techicon (K802156) received a 510(k) decision of Substantially Equivalent on October 10, 1980, 32 days after the submission was received.

What is the product code of K802156?

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