meddevicedb.com FDA Device Reference

MONOSTICON UNI-DOT

K853388 Class II Traditional
Decision Date
1985-08-22
Sponsor / Applicant
Organon, Inc.

Technical Specification

510(k) Submission ID K853388
Product Code KTN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5640
Decision Date 1985-08-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MONOSTICON UNI-DOT received FDA 510(k) clearance under submission number K853388, sponsored by Organon, 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 1985-08-22.

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.