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URIC, UA, OR URIC ACID

K971133 Class I Traditional
Decision Date
1997-04-14
Sponsor / Applicant
Carolina Liquid Chemistries Corp.

Technical Specification

510(k) Submission ID K971133
Product Code KNK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1997-04-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIC, UA, OR URIC ACID received FDA 510(k) clearance under submission number K971133, sponsored by Carolina Liquid Chemistries 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 1997-04-14.

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.