meddevicedb.com FDA Device Reference

HYTEC AUTOIMMUNE KIT (SS-A)

K954392 Class II Traditional
Decision Date
1995-12-26
Sponsor / Applicant
Hycor Biomedical, Inc.

Technical Specification

510(k) Submission ID K954392
Product Code LKJ
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1995-12-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYTEC AUTOIMMUNE KIT (SS-A) received FDA 510(k) clearance under submission number K954392, sponsored by Hycor Biomedical, 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 1995-12-26.

Classification & Regulation

This clearance is catalogued under FDA product code LKJ and 21 CFR 866.5100, within the Immunology review panel as a Class II device.