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G8 AUTOMATED HPLC ANALYZER, MODEL HLC-723 G8

K071132 Class II Traditional
Decision Date
2008-09-16
Sponsor / Applicant
Tosoh Bioscience, Inc.

Technical Specification

510(k) Submission ID K071132
Product Code LCP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7470
Decision Date 2008-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

G8 AUTOMATED HPLC ANALYZER, MODEL HLC-723 G8 received FDA 510(k) clearance under submission number K071132, sponsored by Tosoh Bioscience, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2008-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code LCP and 21 CFR 864.7470, within the Hematology review panel as a Class II device.