Phadecode Xa Inhibitor Assay
FDA 510(k) K792019 · Pharmaseal Div., Baxter Healthcare Corp.
510(k) numberK792019
Submission
- Device name
- Phadecode Xa Inhibitor Assay
- Applicant
- Pharmaseal Div., Baxter Healthcare Corp.
Mchenry, IL, US - Received
- October 9, 1979
- Decision date
- November 5, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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
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|---|---|---|---|
| K242952 | INNOVANCE AntithrombinJBQ · Traditional | Siemens Healthcare Diagnostic Products GmbH | 03/28/2025SE |
| K081769 | Innovance Antithrombin with Models OPFH03, OPFHO5JBQ · Traditional | Siemens Healthcare Diagnostics | 05/28/2009SE |
| K070301 | Hemosil AntithrombinJBQ · Special | Instrumentation Laboratory CO | 02/23/2007SE |
| K062431 | Hemosil Liquid AntithrombinJBQ · Special | Instrumentation Laboratory CO | 09/01/2006SE |
| K043007 | Biophen Antithrombin 2.5, Reference # 221102; Biophen Antithrombin 5, Reference # 221105JBQ · Traditional | Hyphen Biomed | 11/07/2005SE |
| K033775 | Hemosil Liquid Antithrombin XLJBQ · Special | Instrumentation Laboratory CO | 01/02/2004SE |
| K023991 | Chromocheck Antithrombin 25; Chromocheck Antithrombin 50JBQ · Traditional | Precision Biologic | 04/28/2003SE |
| K022550 | Coamatic LR Antithrombin, Note: Lr=Liquid ReagentsJBQ · Traditional | Instrumentation Laboratory CO | 08/27/2002SE |
| K022195 | Coamatic AT-400JBQ · Traditional | Instrumentation Laboratory CO | 08/07/2002SE |
| K994238 | Il Test Liquid AntithrombinJBQ · Traditional | Instrumentation Laboratory CO | 06/23/2000SE |
More from Instrumentation Laboratory CO
| 510(k) | Device | Decision |
|---|---|---|
| K792369 | Hyperalimentation Dressing TrayFRG · Traditional | 12/10/1979SE |
| K792141 | Continuous Flush DeviceKRA · Traditional | 12/05/1979SE |
| K791773 | Ventilator Tube with FilterCAH · Traditional | 10/22/1979SE |
| K791156 | Amipaque Myelogram TrayFMI · Traditional | 07/30/1979SE |
| K790896 | Two-Way Anesthesia FilterCAH · Traditional | 06/05/1979SE |
| K790409 | Low Dead Space Insulin SyringeFMF · Traditional | 04/24/1979SE |
| K782069 | Tray, Auxillary BlockCAZ · Traditional | 01/04/1979SE |
| K781797 | Prep Tray, Preoperative SkinOJU · Traditional | 11/08/1978SE |
| K781680 | Monitoring, Pressure KitDRS · Traditional | 10/06/1978SE |
| K780887 | Improved Disposable Hypodermic NeedleGAA · Traditional | 06/22/1978SE |
Questions and answers
When was Phadecode Xa Inhibitor Assay cleared by the FDA?
Phadecode Xa Inhibitor Assay (K792019) received a 510(k) decision of Substantially Equivalent on November 5, 1979, 27 days after the submission was received.
What is the product code of K792019?
The FDA product code is JBQ – Antithrombin Iii Quantitation, a Class II (moderate risk) device regulated under 21 CFR 864.7060.