meddevicedb.com FDA Device Reference

ALPHA-1-ACID GLYCOPROTEIN (OROSOMUCOID)

K873868 Class I Traditional
Decision Date
1987-10-20
Sponsor / Applicant
Unipath , Ltd.

Technical Specification

510(k) Submission ID K873868
Product Code LKL
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5420
Decision Date 1987-10-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALPHA-1-ACID GLYCOPROTEIN (OROSOMUCOID) received FDA 510(k) clearance under submission number K873868, sponsored by Unipath , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1987-10-20.

Classification & Regulation

This clearance is catalogued under FDA product code LKL and 21 CFR 866.5420, within the Immunology review panel as a Class I device.