Antithrombin Iii, Two Stage Clotting Time Assay

Device Code: 2366

Product Code(s): JPE

Device Classification Information

• Device Type ID: 2366
• Device Name: Antithrombin Iii, Two Stage Clotting Time Assay
• Regulation Description: Antithrombin III Assay.
• Regulation Medical Specialty: Hematology
• Review Panel: Hematology
• Premarket Review: Office Of In Vitro Diagnostics And Radiological Health (OIR)
• Submission Type: 510(k)
• CFR Regulation Number: 864.7060 [🔎]
• FDA Device Classification: Class 2 Medical Device
• Product Code: JPE
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Not Third Party Eligible

Recognized Standards

• 7-159 CLSI H21-A5
  Collection, Transport, And Processing Of Blood Specimens For Testing Plasma-Based Coagulation Assays And Molecular Hemostasis Assays

Total Product Life Cycle

• Device Type ID: 2366
• Device: Antithrombin Iii, Two Stage Clotting Time Assay
• Product Code: JPE
• FDA Device Classification: Class 2 Medical Device
• Regulation Description: Antithrombin III Assay.
• CFR Regulation Number: 864.7060 [🔎]

Device Problems
Low Test Results	1
Total Device Problems	1

TPLC Last Update: 2019-04-02 20:10:31