Phadecode Differential Factor XA1 Assay

FDA 510(k) K770942 · Pharmaseal Div., Baxter Healthcare Corp.

Substantially Equivalent

510(k) numberK770942

Submission

Device name
Phadecode Differential Factor XA1 Assay
Applicant
Pharmaseal Div., Baxter Healthcare Corp.
Mchenry, IL, US
Received
May 24, 1977
Decision date
July 21, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JBQ – Antithrombin Iii Quantitation
Device class
Class II (moderate risk)
Regulation
21 CFR 864.7060
Specialty
Hematology

Other 510(k)s with product code JBQ

510(k)DeviceApplicantDecision
K242952INNOVANCE AntithrombinJBQ · Traditional Siemens Healthcare Diagnostic Products GmbH03/28/2025SE
K081769Innovance Antithrombin with Models OPFH03, OPFHO5JBQ · Traditional Siemens Healthcare Diagnostics05/28/2009SE
K070301Hemosil AntithrombinJBQ · Special Instrumentation Laboratory CO02/23/2007SE
K062431Hemosil Liquid AntithrombinJBQ · Special Instrumentation Laboratory CO09/01/2006SE
K043007Biophen Antithrombin 2.5, Reference # 221102; Biophen Antithrombin 5, Reference # 221105JBQ · Traditional Hyphen Biomed11/07/2005SE
K033775Hemosil Liquid Antithrombin XLJBQ · Special Instrumentation Laboratory CO01/02/2004SE
K023991Chromocheck Antithrombin 25; Chromocheck Antithrombin 50JBQ · Traditional Precision Biologic04/28/2003SE
K022550Coamatic LR Antithrombin, Note: Lr=Liquid ReagentsJBQ · Traditional Instrumentation Laboratory CO08/27/2002SE
K022195Coamatic AT-400JBQ · Traditional Instrumentation Laboratory CO08/07/2002SE
K994238Il Test Liquid AntithrombinJBQ · Traditional Instrumentation Laboratory CO06/23/2000SE

More from Instrumentation Laboratory CO

510(k)DeviceDecision
K792369Hyperalimentation Dressing TrayFRG · Traditional 12/10/1979SE
K792141Continuous Flush DeviceKRA · Traditional 12/05/1979SE
K792019Phadecode Xa Inhibitor AssayJBQ · Traditional 11/05/1979SE
K791773Ventilator Tube with FilterCAH · Traditional 10/22/1979SE
K791156Amipaque Myelogram TrayFMI · Traditional 07/30/1979SE
K790896Two-Way Anesthesia FilterCAH · Traditional 06/05/1979SE
K790409Low Dead Space Insulin SyringeFMF · Traditional 04/24/1979SE
K782069Tray, Auxillary BlockCAZ · Traditional 01/04/1979SE
K781797Prep Tray, Preoperative SkinOJU · Traditional 11/08/1978SE
K781680Monitoring, Pressure KitDRS · Traditional 10/06/1978SE

Questions and answers

When was Phadecode Differential Factor XA1 Assay cleared by the FDA?

Phadecode Differential Factor XA1 Assay (K770942) received a 510(k) decision of Substantially Equivalent on July 21, 1977, 58 days after the submission was received.

What is the product code of K770942?

The FDA product code is JBQ – Antithrombin Iii Quantitation, a Class II (moderate risk) device regulated under 21 CFR 864.7060.