meddevicedb.com FDA Device Reference

UC IMU A

K904125 Class II Traditional
Decision Date
1990-09-24
Sponsor / Applicant
Eucardio Laboratory, Inc.

Technical Specification

510(k) Submission ID K904125
Product Code DER
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5580
Decision Date 1990-09-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UC IMU A received FDA 510(k) clearance under submission number K904125, sponsored by Eucardio Laboratory, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1990-09-24.

Classification & Regulation

This clearance is catalogued under FDA product code DER and 21 CFR 866.5580, within the Immunology review panel as a Class II device.