Creatine Kinase (CK) Reagent Set
FDA 510(k) K881237 · Tech-Neal Scientific, Inc.
510(k) numberK881237
Submission
- Device name
- Creatine Kinase (CK) Reagent Set
- Applicant
- Tech-Neal Scientific, Inc.
Chicago, IL, US - Received
- March 22, 1988
- Decision date
- April 28, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JHX – Fluorometric Method, Cpk Or Isoenzymes
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1215
- Specialty
- Clinical Chemistry
Other 510(k)s with product code JHX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K234005 | Access CK-MBJHX · Traditional | Beckman Coulter, Inc. | 02/16/2024SE |
| K212648 | VITROS Immunodiagnostic Products CK-MB Reagent PackJHX · Traditional | Ortho Clinical Diagnostics | 01/28/2022SE |
| K163462 | AQT90 FLEX Myo Test Kit, AQT90 FLEX CKMB Test Kit, AQT90 FLEXJHX · Traditional | Radiometer Medical Aps | 09/21/2017SE |
| K120326 | AQT90 Flex CKMB Test Kit, AQT90 Flex LQC Multi-Check, Levels 1-3, AQT90 Flex CKMB Cal…JHX · Traditional | Radiometer Medical Aps | 11/21/2012SE |
| K081360 | Pathfast Ck-Mb-Ii, Pathfast Myo-IiJHX · Traditional | Mitsubishi Kagaku Iatron | 08/17/2009SE |
| K051650 | Stratus CS Acute Care MB Isoenzyme of Creatine Kinase (CKMB) Test Pak; Stratus CS Acute…JHX · Traditional | Dade Behring, Inc. | 09/08/2005SE |
| K041596 | Architect Stat Ck-Mb ImmunoassayJHX · Traditional | Fisher Diagnostics | 07/21/2004SE |
| K033747 | Ramp Ck-Mb AssayJHX · Traditional | Response Biomedical Corp. | 05/17/2004SE |
| K034055 | Immulite 2500 Ck-Mb, 2500 Myoglobin, 2500 Stat Troponin IJHX · Special | Diagnostic Products Corp. | 01/21/2004SE |
| K030012 | Ck-Mb and Ck-Mb Calibrators on the Access Immunoassay Systems, Models 386371 and 386372JHX · Special | Beckman Coulter, Inc. | 01/17/2003SE |
More from Beckman Coulter, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K882256 | Magnesium Reagent SetJGJ · Traditional | 08/08/1988SE |
| K882459 | Diazo, Colorimetric BilirubinCIG · Traditional | 08/02/1988SE |
| K881239 | Gamma Glutamyl Transferase Reagent SetJPZ · Traditional | 05/31/1988SE |
| K881241 | Total Bilirubin ReagentCIG · Traditional | 05/27/1988SE |
| K881240 | Chloride Reagent SetCHJ · Traditional | 04/28/1988SE |
| K880237 | CholesterolCHH · Traditional | 04/28/1988SE |
| K880277 | Uric Acid Reagent SetKNK · Traditional | 04/18/1988SE |
| K880845 | Calcium Reagent SetCIC · Traditional | 04/05/1988SE |
| K880844 | Albumin Reagent SetCIX · Traditional | 04/05/1988SE |
| K880843 | Creatinine Reagent Set (Kinetic)CGX · Traditional | 04/05/1988SE |
Questions and answers
When was Creatine Kinase (CK) Reagent Set cleared by the FDA?
Creatine Kinase (CK) Reagent Set (K881237) received a 510(k) decision of Substantially Equivalent on April 28, 1988, 37 days after the submission was received.
What is the product code of K881237?
The FDA product code is JHX – Fluorometric Method, Cpk Or Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1215.