meddevicedb.com FDA Device Reference

IMMUNWELL SJOGREN`S SYNDROME B (LA) ANTIBODY TEST

K911850 Class II Traditional
Decision Date
1991-05-07
Sponsor / Applicant
General Biometrics, Inc.

Technical Specification

510(k) Submission ID K911850
Product Code LKO
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1991-05-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMMUNWELL SJOGREN`S SYNDROME B (LA) ANTIBODY TEST received FDA 510(k) clearance under submission number K911850, sponsored by General Biometrics, 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 1991-05-07.

Classification & Regulation

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