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ROCHE DIAGNOSTICS HITACHI BICARBONATE LIQUID

K032377 Class II Special
Decision Date
2003-08-21
Sponsor / Applicant
Roche Diagnostics Corp.

Technical Specification

510(k) Submission ID K032377
Product Code KHS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1160
Decision Date 2003-08-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ROCHE DIAGNOSTICS HITACHI BICARBONATE LIQUID received FDA 510(k) clearance under submission number K032377, sponsored by Roche Diagnostics Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2003-08-21.

Classification & Regulation

This clearance is catalogued under FDA product code KHS and 21 CFR 862.1160, within the Clinical Chemistry review panel as a Class II device.