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TESTING VISUAL ACUITY

K833778 Class I Traditional
Decision Date
1984-01-04
Sponsor / Applicant
Technical Enginuities Co.

Technical Specification

510(k) Submission ID K833778
Product Code HOX
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1150
Decision Date 1984-01-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TESTING VISUAL ACUITY received FDA 510(k) clearance under submission number K833778, sponsored by Technical Enginuities 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 1984-01-04.

Classification & Regulation

This clearance is catalogued under FDA product code HOX and 21 CFR 886.1150, within the Ophthalmic review panel as a Class I device.