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ROCHE REAGENTS REAGENT FOR URIC ACID

K844986 Class I Traditional
Decision Date
1985-01-18
Sponsor / Applicant
Roche Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K844986
Product Code CDO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1985-01-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ROCHE REAGENTS REAGENT FOR URIC ACID received FDA 510(k) clearance under submission number K844986, sponsored by Roche Diagnostic Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1985-01-18.

Classification & Regulation

This clearance is catalogued under FDA product code CDO and 21 CFR 862.1775, within the Clinical Chemistry review panel as a Class I device.