meddevicedb.com FDA Device Reference

ALPHA-1-ACID GLYCOPROTEIN SERUM, ANTI-HU

K781023 Class I Traditional
Decision Date
1978-08-14
Sponsor / Applicant
Icl Scientific

Technical Specification

510(k) Submission ID K781023
Product Code DEX
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5420
Decision Date 1978-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALPHA-1-ACID GLYCOPROTEIN SERUM, ANTI-HU received FDA 510(k) clearance under submission number K781023, sponsored by Icl Scientific. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1978-08-14.

Classification & Regulation

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