meddevicedb.com FDA Device Reference

TECH. RA-1000SYS-ANALYTES IMMUNOGLOBULIN

K833402 Class II Traditional
Decision Date
1984-01-24
Sponsor / Applicant
Technicon Instruments Corp.

Technical Specification

510(k) Submission ID K833402
Product Code DEW
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1984-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TECH. RA-1000SYS-ANALYTES IMMUNOGLOBULIN received FDA 510(k) clearance under submission number K833402, sponsored by Technicon Instruments Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1984-01-24.

Classification & Regulation

This clearance is catalogued under FDA product code DEW and 21 CFR 866.5510, within the Immunology review panel as a Class II device.