TESTING VISUAL ACUITY— 510(k) K833778

Name: FDA 510(k) clearance K833778
Creator: U.S. Food and Drug Administration
Published: 1984-01-04

Substantially Equivalent

Technical Enginuities Co.

FDA 510(k) clearance K833778 for TESTING VISUAL ACUITY, Substantially Equivalent on 1984-01-04. Applicant: Technical Enginuities Co.. Device class: 1.

Clearance details

Applicant: Technical Enginuities Co.
Product code: Code HOX
Device class: Class 1
Regulation: 21 CFR 886.1150
Advisory panel: Ophthalmic
Date received: 1983-10-27
Decision date: 1984-01-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HOX

view all

K100095 — CENTRAL VISION ANALYZER MODEL 10002010-05-10
K944156 — HEINE LAMBDA 1001995-01-12
K881971 — OCCU-TECH VISION TEST1988-11-25
K883337 — PL 20/20 INFANT VISION TESTER1988-10-31
K882634 — VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE1988-07-15

Data sourced from openFDA. This site is unofficial and independent of the FDA.