CLSI H30-A2

Standard Organization:

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

Recognition Date2004-10-04
Recognition List011
Recognition Number7-105
Extent Complete standard
Standards Orgs CLSI Clinical Laboratory Standards Institute https://clsi.org/
STG InVitro Diagnostics
FDA Tech  Iwona Fijalkowska   FDA/OMPT/CDRH/OIR/DIHD/HEMB/   301-796-6205   iwona.fijalkowska@fda.hhs.gov

Rationale:

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Scope:

This document provides general guidelines for performing the fibrinogen assay in the clinical laboratory. It also includes reporting of results and in vivo and in vitro conditions that may alter results.

Code of Federal Regulations:

Regulation Number Device Name Device Class Product Code
§864.7340 Fibrinogen Standard Class 2 GFX
§864.7340 Plasma, Fibrinogen Control Class 2 GIL
§864.7340 System, Fibrinogen Determination Class 2 KQJ
§864.7340 Test, Fibrinogen Class 2 GIS

FDA Guidance:

Points to Consider for Consider for Collection of Data in Support of In-Vitro Device Submissions for 510(k) Clearance, Issued September 1994.

CLSI C28-A2 How to Define and Determine Reference Intervals in the Clinical Laboratory; Approved Guideline-Second Edition.

CLSI GP39-A6 Tubes and Additives for Venous and Capillary Blood Specimen Collection; Approved Standard-Sixth Edition.

CLSI H3-A4 Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture; Approved Standard-Fourth Edition.

CLSI H21-A5 Collection, Transport, and Processing of Blood Specimens for Coagulation Testing and General Performance of Coagulation Assays; Approved Guideline-Fifth Edition.

CLSI H47-A One-Stage Prothrombin Time (PT) Test and Activated Partial Thromboplastin Time (APTT) Test; Approved Guideline.

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