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URISYS 2400 URINE TEST STRIP

K012397 Class II Traditional
Decision Date
2001-09-26
Sponsor / Applicant
Roche Diagnostics Corp.

Technical Specification

510(k) Submission ID K012397
Product Code JIL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1340
Decision Date 2001-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URISYS 2400 URINE TEST STRIP received FDA 510(k) clearance under submission number K012397, sponsored by Roche Diagnostics Corp.. 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 2001-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code JIL and 21 CFR 862.1340, within the Clinical Chemistry review panel as a Class II device.