meddevicedb.com FDA Device Reference

ANIT-ENA ANTIBODY TEST [SS-B (LA)]

K920384 Class II Traditional
Decision Date
1992-03-30
Sponsor / Applicant
Immco Diagnostics, Inc.

Technical Specification

510(k) Submission ID K920384
Product Code LLL
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1992-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANIT-ENA ANTIBODY TEST [SS-B (LA)] received FDA 510(k) clearance under submission number K920384, sponsored by Immco Diagnostics, 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 1992-03-30.

Classification & Regulation

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