CLSI H7-A3

Standard Organization:

CLSI H7-A3
Procedure for Determining Packed Cell Volume by the Microhematocrit Method - Second Edition; Approved Standard - Third Edition.

Recognition Date2004-10-04
Recognition List011
Recognition Number7-104
Extent Complete standard
Standards Orgs CLSI Clinical Laboratory Standards Institute https://clsi.org/
STG InVitro Diagnostics
FDA Tech  Yvonne Doswell   FDA/OMPT/CDRH/OIR/DIHD/HEMB/   240-402-5025   yvonne.doswell@fda.hhs.gov

Rationale:

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Scope:

The standard is intended for reference use by clinical laboratory personnel and by manufacturers of instruments that determine PCV. The method can also be used (with appropriate precautions as described in the document) in the clinical laboratory for diagnostic purposes, for monitoring a patient's response to therapy, and for evaluating instruments and other methods for determining PCV; the standard should be used for whole blood calibration procedures of hematology analyzers. The document gives detailed specifications of the materials to be used in the procedure, contains information for calibrating the centrifuge and reading device, and includes information on verification of calibration. Expression of results, generally accepted reference values, and potential sources of error are given.

Code of Federal Regulations:

Regulation Number Device Name Device Class Product Code
§864.8165 Calibrator For Hemoglobin And Hematocrit Measurement Class 2 KRZ
§864.6400 Device, Hematocrit Measuring Class 2 JPI
AUTOMATED HEMATOCRIT INSTRUMENT
§864.5600 Instrument, Hematocrit, Automated Class 2 GKF

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


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