Product Classification

• Device: system, multipurpose for in vitro coagulation studies
• Regulation Description: Multipurpose system for in vitro coagulation studies.
• Regulation Medical Specialty: Hematology
• Review Panel: Hematology
• Product Code: JPA
• Premarket Review: Division of Immunology and Hematology Devices (DIHD); Division of Immunology and Hematology Devices (DIHD)
• Submission Type: 510(k)
• Regulation Number: 864.5425
• Device Class: 2
• Total Product Life Cycle (TPLC): TPLC Product Code Report
• GMP Exempt?: No
• Summary Malfunction Reporting: Ineligible
• Implanted Device?: No
• Life-Sustain/Support Device?: No

Recognized Consensus Standards

• 7-159 CLSI H21-A5
  Collection, Transport, and Processing of Blood Specimens for Testing Plasma-Based Coagulation Assays and Molecular Hemostasis Assays
• 7-299 CLSI POCT14 2nd Edition
  Point-of-Care Coagulation Testing and Anticoagulation Monitoring
• 7-301 CLSI GP42 7th Edition
  Collection of Capillary Blood Specimens

Third Party Review

• Eligible for 510(k) Third Party Review Program

Accredited Persons

• aabb
• center for measurement standards of industrial
• global quality and regulatory services
• regulatory technology services, llc