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MILLER/NADLER GLARE TESTER

K832762 Class II Traditional
Decision Date
1983-09-29
Sponsor / Applicant
Titmus Optical, Inc.

Technical Specification

510(k) Submission ID K832762
Product Code HLX
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1630
Decision Date 1983-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MILLER/NADLER GLARE TESTER received FDA 510(k) clearance under submission number K832762, sponsored by Titmus Optical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1983-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code HLX and 21 CFR 886.1630, within the Ophthalmic review panel as a Class II device.