Ultrazyme Plus Ck-I
FDA 510(k) K821883 · Harleco Diagnostics
510(k) numberK821883
Submission
- Device name
- Ultrazyme Plus Ck-I
- Applicant
- Harleco Diagnostics
Mchenry, IL, US - Received
- June 25, 1982
- Decision date
- July 14, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- CGS – Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1215
- Specialty
- Clinical Chemistry
Other 510(k)s with product code CGS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K191296 | Pointe Scientific Creatinine Kinase (CK) Reagent SetCGS · Traditional | Medtest DX | 08/11/2020SE |
| K182702 | SEKURE Creatine Kinase AssayCGS · Traditional | Sekisui Diagnostics P.E.I., Inc. | 04/17/2019SE |
| K160724 | ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 CalibratorCGS · Traditional | Siemens Healthcare Diagnostics, Inc. | 09/07/2016SE |
| K123977 | Randox Liquid Ck-Mb, Randox Ck-Mb CalibratorCGS · Traditional | Randox Laboratories, Ltd. | 11/21/2013SE |
| K112416 | CPK ReagentCGS · Traditional | Vital Diagnostics (Manufacturing) Ptyltd | 11/09/2011SE |
| K083465 | Dimension Vista Creatine Kinase Flex Reagent Cartridge and Dimension Vista Creatine…CGS · Special | Siemens Healthcare Diagnostics | 02/27/2009SE |
| K081731 | Dimension Cki Flex Reagent Cartridge, Dimension Mbi Flex Reagent Cartridge, and Cki/Mbi…CGS · Traditional | Siemens Healthcare Diagnostics | 08/29/2008SE |
| K072548 | Creatine Kinase Liquid Reagent, Model C519-440CGS · Traditional | Teco Diagnostics | 04/18/2008SE |
| K062737 | Cardiac Markers on Abx Pentra 400 Clinical Chemistry AnalyzerCGS · Traditional | Horiba Abx | 06/12/2007SE |
| K051648 | Spotchem II Inoganic Phosphorus, CPK and Uric Acid TestsCGS · Traditional | Arkray, Inc. | 01/31/2006SE |
More from Arkray, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K823147 | Uric Acid Standard, 8MG/DL #65078JIS · Traditional | 11/22/1982SE |
| K822852 | Triglyceride CalibratorJIT · Traditional | 10/27/1982SE |
| K822323 | Ultrachem Bun-Uv, 65080 & 65081CDW · Traditional | 09/02/1982SE |
| K821882 | Ultrazyme Plus GPTCKA · Traditional | 07/14/1982SE |
| K821881 | Ultrachem CreaCGX · Traditional | 07/14/1982SE |
| K821880 | Ultra Chem AlbCIX · Traditional | 07/14/1982SE |
| K821879 | Ultrachem T.P.CEX · Traditional | 07/14/1982SE |
| K821878 | Ultrazyme Plus LDHCFJ · Traditional | 07/14/1982SE |
| K821877 | Ultrazyme Plus HBDJMK · Traditional | 07/14/1982SE |
| K821873 | Ultrachem T-BiliCIG · Traditional | 07/14/1982SE |
Questions and answers
When was Ultrazyme Plus Ck-I cleared by the FDA?
Ultrazyme Plus Ck-I (K821883) received a 510(k) decision of Substantially Equivalent on July 14, 1982, 19 days after the submission was received.
What is the product code of K821883?
The FDA product code is CGS – Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1215.