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IMMUNODOT AUTOIMMUNITY SCREENING PANEL 2

K900072 Class II Traditional
Decision Date
1990-01-24
Sponsor / Applicant
General Biometrics, Inc.

Technical Specification

510(k) Submission ID K900072
Product Code LJM
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1990-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMMUNODOT AUTOIMMUNITY SCREENING PANEL 2 received FDA 510(k) clearance under submission number K900072, 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 1990-01-24.

Classification & Regulation

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