meddevicedb.com FDA Device Reference

LIQUICHEK URINE CHEMISTRY CONTROL

K121794 Class I Traditional
Decision Date
2012-07-11
Sponsor / Applicant
Bio-Rad, Diagnostics Grp.

Technical Specification

510(k) Submission ID K121794
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2012-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIQUICHEK URINE CHEMISTRY CONTROL received FDA 510(k) clearance under submission number K121794, sponsored by Bio-Rad, Diagnostics Grp.. 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 2012-07-11.

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.