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URIC ACID REAGENT SET

K834045 Class I Traditional
Decision Date
1984-01-30
Sponsor / Applicant
Sterling Biochemical, Inc.

Technical Specification

510(k) Submission ID K834045
Product Code KNK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1984-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIC ACID REAGENT SET received FDA 510(k) clearance under submission number K834045, sponsored by Sterling Biochemical, 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 1984-01-30.

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.