meddevicedb.com FDA Device Reference

DORC LIGHTWEIGHT BINOCULAR OPHTHALMOSCOP

K830215 Class II Traditional
Decision Date
1983-03-09
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K830215
Product Code HLJ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1570
Decision Date 1983-03-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DORC LIGHTWEIGHT BINOCULAR OPHTHALMOSCOP received FDA 510(k) clearance under submission number K830215, sponsored by Jedmed Instrument Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1983-03-09.

Classification & Regulation

This clearance is catalogued under FDA product code HLJ and 21 CFR 886.1570, within the Ophthalmic review panel as a Class II device.