Creatinine2
FDA 510(k) K210452 · Abbott Ireland Diagnostics Division
510(k) numberK210452
Submission
- Device name
- Creatinine2
- Applicant
- Abbott Ireland Diagnostics Division
Longford, IE - Received
- February 16, 2021
- Decision date
- March 22, 2022
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- CGX – Alkaline Picrate, Colorimetry, Creatinine
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1225
- Specialty
- Clinical Chemistry
Other 510(k)s with product code CGX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252206 | Nova Allegro UACR Assay, Nova Allegro AnalyzerCGX · Dual Track | Nova Biomedical Corporation | 01/09/2026SE |
| K251058 | Tru Kidney Health Test Panel; Tru AnalyzerCGX · Traditional | Truvian Health | 11/26/2025SE |
| K242685 | Atellica® CH Creatinine_3 (Crea3)CGX · Traditional | Siemens Healthcare Diagnostics, Inc. | 12/04/2024SE |
| K221813 | Nova Allegro UACR Assay, Nova Allegro AnalyzerCGX · Dual Track | Nova Biomedical Corporation | 11/19/2024SE |
| K161494 | Atellica CH Creatinine_2 (Crea_2), Atellica CH Chemistry Calibrator (CHEM CAL)CGX · Traditional | Siemens Healthcare Diagnostics, Inc. | 11/15/2016SE |
| K132638 | Dimension Creatinine (CRE2) Flex Reagent CartridgeCGX · Traditional | Siemens Healthcare Diagnostics, Inc. | 01/27/2014SE |
| K133728 | Dimension Vista Creatinine (CRE2) Flex Reagent CartridgeCGX · Traditional | Siemens Healthcare Diagnostics, Inc. | 01/24/2014SE |
| K123586 | Easyra Creatinine ReagentCGX · Special | Medica Corporation | 05/15/2013SE |
| K110530 | Abx Pentra Creatinine 120 CP; Abx Pentra Multical; Abx Pentra N Control; Abx Pentra P…CGX · Abbreviated | Horiba Abx SAS | 04/30/2012SE |
| K083809 | CreatinineCGX · Special | Abbott Laboratories | 04/07/2009SE |
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| 510(k) | Device | Decision |
|---|---|---|
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| K203597 | Cholesterol2CHH · Traditional | 06/30/2022SE |
| K203771 | Urea Nitrogen2CDQ · Traditional | 05/31/2022SE |
| K210633 | Amylase2JFJ · Traditional | 05/26/2022SE |
| K203530 | Albumin BCP2CJW · Traditional | 03/18/2022SE |
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Questions and answers
When was Creatinine2 cleared by the FDA?
Creatinine2 (K210452) received a 510(k) decision of Substantially Equivalent on March 22, 2022, 399 days after the submission was received.
What is the product code of K210452?
The FDA product code is CGX – Alkaline Picrate, Colorimetry, Creatinine, a Class II (moderate risk) device regulated under 21 CFR 862.1225.