meddevicedb.com FDA Device Reference

IRI SPEC URINALYSIS CONTROL

K832713 Class I Traditional
Decision Date
1983-12-22
Sponsor / Applicant
Intl. Remote Imaging Systems

Technical Specification

510(k) Submission ID K832713
Product Code JJW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1983-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IRI SPEC URINALYSIS CONTROL received FDA 510(k) clearance under submission number K832713, sponsored by Intl. Remote Imaging Systems. 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 1983-12-22.

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.