CLSI GP34-A (Replaces GP34-P)

Standard Organization:

CLSI GP34-A (Replaces GP34-P)
Validation and Verfication of Tubes for Venous and Capillary Blood Specimen Collection; Approved Guidance

Recognition Date2012-03-16
Recognition List028
Recognition Number7-225
Extent Complete standard
Standards Orgs CLSI Clinical Laboratory Standards Institute https://clsi.org/
STG InVitro Diagnostics
FDA Tech  Yung Chan   FDA/OMPT/CDRH/OIR/DCTD/   301-796-6138   yung.chan@fda.hhs.gov

Rationale:

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Scope:

This document is a guideline for manufacturers of venous and capillary blood collection tubes and users of blood collection tubes for serum, plasma, and whole blood testing. GP34 provides guidelines for validation and verification of test (examination) performance.

Code of Federal Regulations:

Regulation Number Device Name Device Class Product Code
§862.1675 Tubes, Vials, Systems, Serum Separators, Blood Collection Class 2 JKA

FDA Guidance:

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


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