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PRECINORM PROTEINS IN URINE/CSF (PUC) AND PRECIPATH PUC

K050026 Class II Special
Decision Date
2005-01-31
Sponsor / Applicant
Roche Diagnostics

Technical Specification

510(k) Submission ID K050026
Product Code JIX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 2005-01-31
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRECINORM PROTEINS IN URINE/CSF (PUC) AND PRECIPATH PUC received FDA 510(k) clearance under submission number K050026, sponsored by Roche Diagnostics. 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 2005-01-31.

Classification & Regulation

This clearance is catalogued under FDA product code JIX and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.