Multi-Lipid Calibrator

FDA 510(k) K042550 · Wako Chemicals USA, Inc.

Substantially Equivalent

510(k) numberK042550

Submission

Device name
Multi-Lipid Calibrator
Applicant
Wako Chemicals USA, Inc.
Richmond, VA, US
Received
September 20, 2004
Decision date
November 8, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JIX – Calibrator, Multi-Analyte Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

Other 510(k)s with product code JIX

510(k)DeviceApplicantDecision
K161140VITROS Chemistry Products Calibrator Kit 3JIX · Abbreviated Ortho-Clinical Diagnostics, Inc.05/20/2016SE
K153365ADVIA Chemistry Enzyme 1 Calibrator, ADVIA Chemistry Enzyme 2 CalibratorJIX · Traditional Siemens Healthcare Diagnostics, Inc.12/18/2015SE
K151552ELITech Clinical Systems ELICAL 2, ELITech Clinical Systems ELITROL I, ELITech Clinical…JIX · Abbreviated Elitechgroup07/08/2015SE
K140790Dimension Vista Chemistry 1 Calibrator (CHEM 1 CAL), Dimension Vista Magnesium Flex…JIX · Traditional Siemens Healthcare Diagnostics06/15/2015SE
K141388System CalibraterJIX · Abbreviated Beckman Coulter Ireland, Inc.07/11/2014SE
K133330C.F.A.S. Proteins, C.F.A.S. Pac, Precicontrol Clinchem Multi 1 & 2, Precinorm Protein &…JIX · Special Roche Diagnostics11/26/2013SE
K130765Elitech Clinical Systems Elical 2; Elitech Clinical Systems Elitrol I, Elitech Clinical…JIX · Abbreviated Elitechgroup04/04/2013SE
K123321Dimension Chemistry III CalibratoryJIX · Traditional Siemens Healthcare Diagnostics02/15/2013SE
K123372Abbott Lipid Multi Constituent CalibratorJIX · Traditional Abbott Laboratories01/14/2013SE
K122398Rapidpoint 500 System Measurement Cartridge with CalibratorsJIX · Traditional Siemens Healthcare Diagnostics, Inc.10/12/2012SE

More from Siemens Healthcare Diagnostics, Inc.

510(k)DeviceDecision
K100464Utaswako I30 (Includes Accessories), Utaswako AFP-L3, Calibrator Set, Control L, Control…NSF · Traditional 02/23/2011SE
K080125Apolowako T-Cho, Hdl-C, TG and Analyzer, Models 993-23501, 999-23601, 995-23701 and…LBS · Traditional 07/18/2008SE
K080123Apolowako HBA1C, Glucose and Analyzer, Models 993-24601, 991-24401 and 993-25201CFR · Traditional 07/17/2008SE
K061775Wako L-Type Creatinine-M Test, and Wako Creatinine CalibratorJFY · Traditional 02/23/2007SE
K062368Wako Lba DCP Test System, Model 993-05301; DCP Control Set, Model 995-0551; DCP…OAU · Traditional 01/31/2007SE
K053132Wako Direct Bilirubin V, Models 996-23591, 412-22901, 992-23691, 998-23791JFM · Traditional 12/30/2005SE
K053131Wako Total Bilirubin V, Models 410-22701, 998-23291, 416-22801, 990-23191JFM · Traditional 12/30/2005SE
K042551Multi-Chem Calibrator aJIX · Traditional 11/16/2004SE
K042549Multi Chem Cal BJIX · Traditional 11/08/2004SE
K040918Wako Lipid Control, Level 1 and Level 2JJX · Traditional 05/17/2004SE

Questions and answers

When was Multi-Lipid Calibrator cleared by the FDA?

Multi-Lipid Calibrator (K042550) received a 510(k) decision of Substantially Equivalent on November 8, 2004, 49 days after the submission was received.

What is the product code of K042550?

The FDA product code is JIX – Calibrator, Multi-Analyte Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.1150.