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URIC ACID (URICASE) REAGENT, UNIVERSAL

K912028 Class I Traditional
Decision Date
1991-12-18
Sponsor / Applicant
Enzyme Technology, Inc.

Technical Specification

510(k) Submission ID K912028
Product Code KNK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1991-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIC ACID (URICASE) REAGENT, UNIVERSAL received FDA 510(k) clearance under submission number K912028, sponsored by Enzyme Technology, 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 1991-12-18.

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.