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COLUMNMATE BETA THAL HBA2 CONTROL-ABNORMAL

K923317 Class II Traditional
Decision Date
1992-08-25
Sponsor / Applicant
Helena Laboratories

Technical Specification

510(k) Submission ID K923317
Product Code JPD
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7400
Decision Date 1992-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COLUMNMATE BETA THAL HBA2 CONTROL-ABNORMAL received FDA 510(k) clearance under submission number K923317, sponsored by Helena Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1992-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code JPD and 21 CFR 864.7400, within the Hematology review panel as a Class II device.