meddevicedb.com FDA Device Reference

MONO SCREENING TEST

K830531 Class II Traditional
Decision Date
1983-03-17
Sponsor / Applicant
Tago, Inc.

Technical Specification

510(k) Submission ID K830531
Product Code KTN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5640
Decision Date 1983-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MONO SCREENING TEST received FDA 510(k) clearance under submission number K830531, sponsored by Tago, 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 1983-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code KTN and 21 CFR 866.5640, within the Immunology review panel as a Class II device.