meddevicedb.com FDA Device Reference

URITEST - NITRITE IN URINE TEST

K954685 Class I Traditional
Decision Date
1996-07-22
Sponsor / Applicant
Tcpi, Inc.

Technical Specification

510(k) Submission ID K954685
Product Code JMT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1510
Decision Date 1996-07-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URITEST - NITRITE IN URINE TEST received FDA 510(k) clearance under submission number K954685, sponsored by Tcpi, Inc.. 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 1996-07-22.

Classification & Regulation

This clearance is catalogued under FDA product code JMT and 21 CFR 862.1510, within the Clinical Chemistry review panel as a Class I device.