meddevicedb.com FDA Device Reference

IMMUCHEM GAL-MW EA

K951329 Class I Traditional
Decision Date
1995-11-09
Sponsor / Applicant
Icn Pharmaceuticals, Inc.

Technical Specification

510(k) Submission ID K951329
Product Code JIA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1310
Decision Date 1995-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMMUCHEM GAL-MW EA received FDA 510(k) clearance under submission number K951329, sponsored by Icn Pharmaceuticals, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1995-11-09.

Classification & Regulation

This clearance is catalogued under FDA product code JIA and 21 CFR 862.1310, within the Clinical Chemistry review panel as a Class I device.