Liason XL1,25 Dihydroxyvitamin D; Control Set, Calibration Verifiers
FDA 510(k) K141463 · DiaSorin, Inc.
510(k) numberK141463
Submission
- Device name
- Liason XL1,25 Dihydroxyvitamin D; Control Set, Calibration Verifiers
- Applicant
- DiaSorin, Inc.
Stillwater, MN, US - Received
- June 3, 2014
- Decision date
- December 10, 2014
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MRG – System, Test, Vitamin D
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1825
- Specialty
- Clinical Chemistry
Other 510(k)s with product code MRG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K232587 | MAGLUMI 25-OH Vitamin D, MAGLUMI X3 Fully-auto chemiluminescence immunoassay analyzerMRG · Traditional | Shenzhen New Industries Biomedical Engineering… | 04/12/2024SE |
| K221817 | ALFIS Vitamin D, ALFIS-3 AnalyzerMRG · Traditional | Immunostics Inc., | 09/22/2023SE |
| K223503 | Access 25(OH) Vitamin D TotalMRG · Traditional | Beckman Coulter, Inc. | 01/19/2023SE |
| K210901 | Elecsys Vitamin D total IIIMRG · Traditional | Roche Diagnostics | 09/01/2021SE |
| K200509 | ADVIA Centaur Vitamin D Total (VitD)MRG · Traditional | Siemens Healthcare Diagnostics, Inc. | 05/29/2020SE |
| K191499 | MAGLUMI 2000 25-OH Vitamin DMRG · Traditional | Shenzhen New Industries Biomedical Engineering… | 08/01/2019SE |
| K180577 | BioPlex 2200 25-OH Vitamin D KitMRG · Traditional | Bio-Rad Laboratories | 06/22/2018SE |
| K172992 | Diazyme EZ Vitamin D AssayMRG · Traditional | Diazyme Laboratories | 01/11/2018SE |
| K162298 | LOCI Total Vitamin D Total Assay, LOCI VITD CALMRG · Traditional | Siemens Healthcare Diagnostics | 03/16/2017SE |
| K162840 | Elecsys Vitamin D total II, Vitamin D total II CalSet, PreciControl Vitamin D total II…MRG · Traditional | Roche Diagnostics | 02/08/2017SE |
More from Roche Diagnostics
| 510(k) | Device | Decision |
|---|---|---|
| K260770 | LIAISON Murex HBsAg Qual; LIAISON XL; LIAISON diluteXLOM · Traditional | 06/04/2026SE |
| K231214 | LIAISON VZV IgG HT, LIAISON Control VZV IgG HTLFY · Traditional | 10/27/2023SE |
| K223403 | LIAISON Anti-HAV; LIAISON XSLOL · Special | 12/09/2022SE |
| K213858 | LIAISON Calprotectin, LIAISON Q.S.E.T. Device PlusNXO · Traditional | 07/26/2022SE |
| K213936 | LIAISON MeMed BV, LIAISON MeMed BV Control SetQPS · Traditional | 07/14/2022SE |
| K193650 | LIAISON FerritinDBF · Traditional | 09/14/2021SE |
| K202574 | LIAISON Lyme IgG, LIAISON Lyme IgG Control Set, LIAISON Lyme Total Antibody PlusLSR · Traditional | 02/18/2021SE |
| K202573 | LIAISON Lyme IgM, LIAISON Lyme IgM Control Set, LIAISON Lyme Total Antibody PlusLSR · Traditional | 02/18/2021SE |
| K210272 | LIAISON Anti-HAVLOL · Special | 02/09/2021SE |
| K201908 | LIAISON Testosterone xtCDZ · Special | 10/15/2020SE |
Questions and answers
When was Liason XL1,25 Dihydroxyvitamin D; Control Set, Calibration Verifiers cleared by the FDA?
Liason XL1,25 Dihydroxyvitamin D; Control Set, Calibration Verifiers (K141463) received a 510(k) decision of Substantially Equivalent on December 10, 2014, 190 days after the submission was received.
What is the product code of K141463?
The FDA product code is MRG – System, Test, Vitamin D, a Class II (moderate risk) device regulated under 21 CFR 862.1825.