meddevicedb.com FDA Device Reference

OPHTHALMO ECHOGRAPH MODEL ZD255G

K802635 Class II Traditional
Decision Date
1981-04-23
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K802635
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 1981-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPHTHALMO ECHOGRAPH MODEL ZD255G received FDA 510(k) clearance under submission number K802635, sponsored by Jedmed Instrument Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1981-04-23.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.