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MAGNIFYING SPECTACLES W/PLASTIC LENSES

K844716 Class I Traditional
Decision Date
1985-01-03
Sponsor / Applicant
Gazelle Corp.

Technical Specification

510(k) Submission ID K844716
Product Code HOI
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5840
Decision Date 1985-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAGNIFYING SPECTACLES W/PLASTIC LENSES received FDA 510(k) clearance under submission number K844716, sponsored by Gazelle 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 1985-01-03.

Classification & Regulation

This clearance is catalogued under FDA product code HOI and 21 CFR 886.5840, within the Ophthalmic review panel as a Class I device.