Creatinine Reagents B6370-13

FDA 510(k) K831628 · American Scientific Products

Substantially Equivalent

510(k) numberK831628

Submission

Device name
Creatinine Reagents B6370-13
Applicant
American Scientific Products
Mchenry, IL, US
Received
May 20, 1983
Decision date
July 6, 1983
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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K242685Atellica® CH Creatinine_3 (Crea3)CGX · Traditional Siemens Healthcare Diagnostics, Inc.12/04/2024SE
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K132638Dimension Creatinine (CRE2) Flex Reagent CartridgeCGX · Traditional Siemens Healthcare Diagnostics, Inc.01/27/2014SE
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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
K864824Infectious Tissue Kit · Traditional 12/24/1986SE
K844042Blood Dilution VialGKL · Traditional 10/23/1984SE
K831634Glucose Reagent B6360-11CGA · Traditional 07/19/1983SE
K831626Urea Nitrogen-Bun-Reagents B6370-11ACDQ · Traditional 07/07/1983SE
K831625Urea Nitrogen-Bun-Reagents B6360-12CDQ · Traditional 07/07/1983SE
K831627Creatinine Reagents B6360-10CGX · Traditional 07/06/1983SE
K831624Glucose Reagent KITS-B6370-10ACGA · Traditional 07/06/1983SE
K831571RotorJJG · Traditional 06/30/1983SE
K831569Reagent CupsJJG · Traditional 06/30/1983SE
K822799Streptacoccus Co-Agglutination KitGTP · Traditional 12/19/1982SE

Questions and answers

When was Creatinine Reagents B6370-13 cleared by the FDA?

Creatinine Reagents B6370-13 (K831628) received a 510(k) decision of Substantially Equivalent on July 6, 1983, 47 days after the submission was received.

What is the product code of K831628?

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