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POCKET OPHTHALMOSCOPE GH

K843897 Class II Traditional
Decision Date
1984-11-27
Sponsor / Applicant
Design Med. Corp.

Technical Specification

510(k) Submission ID K843897
Product Code HLJ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1570
Decision Date 1984-11-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POCKET OPHTHALMOSCOPE GH received FDA 510(k) clearance under submission number K843897, sponsored by Design Med. Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1984-11-27.

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.