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WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA

K023550 Class I Traditional
Decision Date
2002-12-09
Sponsor / Applicant
Wiener Laboratories Saic

Technical Specification

510(k) Submission ID K023550
Product Code KNK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 2002-12-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA received FDA 510(k) clearance under submission number K023550, sponsored by Wiener Laboratories Saic. 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 2002-12-09.

Classification & Regulation

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