Product Classification

• Device: system, fibrinogen determination
• Regulation Description: Fibrinogen determination system.
• Regulation Medical Specialty: Hematology
• Review Panel: Hematology
• Product Code: KQJ
• Premarket Review: Division of Immunology and Hematology Devices (DIHD); Division of Immunology and Hematology Devices (DIHD)
• Submission Type: 510(k)
• Regulation Number: 864.7340
• Device Class: 2
• Total Product Life Cycle (TPLC): TPLC Product Code Report
• GMP Exempt?: No
• Summary Malfunction Reporting: Eligible
• Implanted Device?: No
• Life-Sustain/Support Device?: No

Recognized Consensus Standard

• 7-105 CLSI H30-A2
  Procedure for the Determination of Fibrinogen in Plasma; Approved Guideline Second Edition

Third Party Review

• Eligible for 510(k) Third Party Review Program

Accredited Persons

• aabb
• global quality and regulatory services
• regulatory technology services, llc