HMS Purple and Black Heparin Cartridges & Control

FDA 510(k) K922031 · Medtronic Hemotec, Inc.

Substantially Equivalent

510(k) numberK922031

Submission

Device name
HMS Purple and Black Heparin Cartridges & Control
Applicant
Medtronic Hemotec, Inc.
Englewood, CO, US
Received
May 1, 1992
Decision date
July 21, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JOX – Analyzer, Heparin, Automated
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5680
Specialty
Hematology

Other 510(k)s with product code JOX

510(k)DeviceApplicantDecision
K111339Hemostasis Managment System Plus (Hms-Plus)JOX · Special Medtronic, Inc.06/08/2011SE
K102953Heparin Dose Response CartridgeJOX · Special Medtronic, Inc.11/04/2010SE
K101271Hemostasis Management System Plus (HMS Plus ), Model 305 XXJOX · Special Medtronic, Inc.10/13/2010SE
K051040Heparin Dose Response Controls, Model 306-20 PorJOX · Special Medtronic Perfusion Systems05/24/2005SE
K043080Heparin Dose Response Controls, Model 306-20 PorJOX · Special Medtronic Vascular12/03/2004SE
K042070Heparin Dose Response Cartridge, Model 304-20JOX · Special Medtronic Vascular10/01/2004SE
K993519Rapidpoint Accent, Model 2000, Rapidpoint Coag Heparin Titration Test, Rapidpoint Coag…JOX · Traditional Cardiovascular Diagnostics, Inc.01/14/2000SE
K911240Hepcon HMS with Body Surface Area CalculationJOX · Traditional Hemotech, Inc.07/17/1991SE
K894317Hemotec Hepcon HMS Coagulation System & Access.JOX · Traditional Hemotec, Inc.09/05/1989SE
K854377Hemotec CV Whole Blood Coagulation ControlsJOX · Traditional Hemotec, Inc.12/04/1985SE

More from Hemotec, Inc.

510(k)DeviceDecision
K954202Platelet Function Test Assay Cartridges for the Hepcon HMSJPA · Traditional 06/20/1996SE
K944115Heparin Assay Cartridges and ControlsGFT · Traditional 03/24/1995SE
K940426Medtronic Hemotec Act II Automated Coagulation TimerGKN · Traditional 09/20/1994SE
K923594Clottrac Coagulation ControlJBP · Traditional 09/21/1992SE

Questions and answers

When was HMS Purple and Black Heparin Cartridges & Control cleared by the FDA?

HMS Purple and Black Heparin Cartridges & Control (K922031) received a 510(k) decision of Substantially Equivalent on July 21, 1992, 81 days after the submission was received.

What is the product code of K922031?

The FDA product code is JOX – Analyzer, Heparin, Automated, a Class II (moderate risk) device regulated under 21 CFR 864.5680.