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URIC-ACID TEST ENZYMATIC COLORIMETRIC

K831864 Class I Traditional
Decision Date
1983-07-22
Sponsor / Applicant
Stanbio Laboratory

Technical Specification

510(k) Submission ID K831864
Product Code KNK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1983-07-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIC-ACID TEST ENZYMATIC COLORIMETRIC received FDA 510(k) clearance under submission number K831864, sponsored by Stanbio Laboratory. 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 1983-07-22.

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.