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URIC ACID TEST

K811810 Class I Traditional
Decision Date
1981-07-15
Sponsor / Applicant
Environmental Chemical Specialties

Technical Specification

510(k) Submission ID K811810
Product Code KNK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1981-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIC ACID TEST received FDA 510(k) clearance under submission number K811810, sponsored by Environmental Chemical Specialties. 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 1981-07-15.

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.