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URIC ACID REAGENT SET (COLORIMETRIC)

K860142 Class I Traditional
Decision Date
1986-02-11
Sponsor / Applicant
Sterling Diagnostics, Inc.

Technical Specification

510(k) Submission ID K860142
Product Code LFQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1986-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIC ACID REAGENT SET (COLORIMETRIC) received FDA 510(k) clearance under submission number K860142, sponsored by Sterling Diagnostics, 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 1986-02-11.

Classification & Regulation

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