meddevicedb.com FDA Device Reference

UA-CELLULAR COMPLETE

K131444 Class I Traditional
Decision Date
2014-01-29
Sponsor / Applicant
Streck

Technical Specification

510(k) Submission ID K131444
Product Code JJW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2014-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UA-CELLULAR COMPLETE received FDA 510(k) clearance under submission number K131444, sponsored by Streck. 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 2014-01-29.

Classification & Regulation

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