Vitros Chemistry Products Ci-Slides, Calibrator Kit 2, Model(S) 844-5207, 166-2659
FDA 510(k) K071801 · Ortho-Clinical Diagnostics, Inc.
510(k) numberK071801
Submission
- Device name
- Vitros Chemistry Products Ci-Slides, Calibrator Kit 2, Model(S) 844-5207, 166-2659
- Applicant
- Ortho-Clinical Diagnostics, Inc.
Rochester, NY, US - Received
- July 2, 2007
- Decision date
- July 20, 2007
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- JIX – Calibrator, Multi-Analyte Mixture
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1150
- Specialty
- Clinical Chemistry
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| K140790 | Dimension Vista Chemistry 1 Calibrator (CHEM 1 CAL), Dimension Vista Magnesium Flex…JIX · Traditional | Siemens Healthcare Diagnostics | 06/15/2015SE |
| K141388 | System CalibraterJIX · Abbreviated | Beckman Coulter Ireland, Inc. | 07/11/2014SE |
| K133330 | C.F.A.S. Proteins, C.F.A.S. Pac, Precicontrol Clinchem Multi 1 & 2, Precinorm Protein &…JIX · Special | Roche Diagnostics | 11/26/2013SE |
| K130765 | Elitech Clinical Systems Elical 2; Elitech Clinical Systems Elitrol I, Elitech Clinical…JIX · Abbreviated | Elitechgroup | 04/04/2013SE |
| K123321 | Dimension Chemistry III CalibratoryJIX · Traditional | Siemens Healthcare Diagnostics | 02/15/2013SE |
| K123372 | Abbott Lipid Multi Constituent CalibratorJIX · Traditional | Abbott Laboratories | 01/14/2013SE |
| K122398 | Rapidpoint 500 System Measurement Cartridge with CalibratorsJIX · Traditional | Siemens Healthcare Diagnostics, Inc. | 10/12/2012SE |
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Questions and answers
When was Vitros Chemistry Products Ci-Slides, Calibrator Kit 2, Model(S) 844-5207, 166-2659 cleared by the FDA?
Vitros Chemistry Products Ci-Slides, Calibrator Kit 2, Model(S) 844-5207, 166-2659 (K071801) received a 510(k) decision of Substantially Equivalent on July 20, 2007, 18 days after the submission was received.
What is the product code of K071801?
The FDA product code is JIX – Calibrator, Multi-Analyte Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.1150.