meddevicedb.com FDA Device Reference

TECHNA VISION AUTO-PERIMETER

K853290 Class I Traditional
Decision Date
1985-11-12
Sponsor / Applicant
Techna Vision

Technical Specification

510(k) Submission ID K853290
Product Code HPT
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1605
Decision Date 1985-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TECHNA VISION AUTO-PERIMETER received FDA 510(k) clearance under submission number K853290, sponsored by Techna Vision. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1985-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code HPT and 21 CFR 886.1605, within the Ophthalmic review panel as a Class I device.