meddevicedb.com FDA Device Reference

RRT SYSTEM LASER REFLECTOMETER ANALYZER

K873407 Class I Traditional
Decision Date
1987-09-23
Sponsor / Applicant
Incstar Corp.

Technical Specification

510(k) Submission ID K873407
Product Code JZW
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.4540
Decision Date 1987-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RRT SYSTEM LASER REFLECTOMETER ANALYZER received FDA 510(k) clearance under submission number K873407, sponsored by Incstar 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 1987-09-23.

Classification & Regulation

This clearance is catalogued under FDA product code JZW and 21 CFR 866.4540, within the Immunology review panel as a Class I device.