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URIC ACID, BOUND ENZYME

K790092 Class I Traditional
Decision Date
1979-03-12
Sponsor / Applicant
Technicon Instruments Corp.

Technical Specification

510(k) Submission ID K790092
Product Code KNK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1979-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIC ACID, BOUND ENZYME received FDA 510(k) clearance under submission number K790092, sponsored by Technicon Instruments 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 1979-03-12.

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.