meddevicedb.com FDA Device Reference

IMAGE DEFLECTOR

K833669 Class I Traditional
Decision Date
1984-03-27
Sponsor / Applicant
Michael Onufryk

Technical Specification

510(k) Submission ID K833669
Product Code HPA
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1415
Decision Date 1984-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMAGE DEFLECTOR received FDA 510(k) clearance under submission number K833669, sponsored by Michael Onufryk. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1984-03-27.

Classification & Regulation

This clearance is catalogued under FDA product code HPA and 21 CFR 886.1415, within the Ophthalmic review panel as a Class I device.