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URISCAN OPTIMA II URINE ANALYZER

K050801 Class II Special
Decision Date
2005-04-20
Sponsor / Applicant
Yd Diagnostics

Technical Specification

510(k) Submission ID K050801
Product Code JIL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1340
Decision Date 2005-04-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URISCAN OPTIMA II URINE ANALYZER received FDA 510(k) clearance under submission number K050801, sponsored by Yd 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 2005-04-20.

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.