meddevicedb.com FDA Device Reference

URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & II

K881275 Class I Traditional
Decision Date
1988-05-16
Sponsor / Applicant
Fisher Scientific Co., LLC

Technical Specification

510(k) Submission ID K881275
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1988-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & II received FDA 510(k) clearance under submission number K881275, sponsored by Fisher Scientific Co., LLC. 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 1988-05-16.

Classification & Regulation

This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.