System, Fibrinogen Determination

Device Code: 2383

Product Code(s): KQJ

Device Classification Information

• Device Type ID: 2383
• Device Name: System, Fibrinogen Determination
• Regulation Description: Fibrinogen Determination System.
• 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: 864.7340 [🔎]
• FDA Device Classification: Class 2 Medical Device
• Product Code: KQJ
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Eligible For Accredited Persons Expansion Pilot Program

Recognized Standards

• 7-105 CLSI H30-A2
  Procedure For The Determination Of Fibrinogen In Plasma; Approved Guideline Second Edition

Total Product Life Cycle

• Device Type ID: 2383
• Device: System, Fibrinogen Determination
• Product Code: KQJ
• FDA Device Classification: Class 2 Medical Device
• Regulation Description: Fibrinogen Determination System.
• CFR Regulation Number: 864.7340 [🔎]

Recalls
Manufacturer		Recall Class	Date Posted
1	Fisher Diagnostics	II	Jul-25-2017

TPLC Last Update: 2019-04-02 20:10:51