VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE— 510(k) K882634

Name: FDA 510(k) clearance K882634
Creator: U.S. Food and Drug Administration
Published: 1988-07-15

Substantially Equivalent

Vistech Consultants, Inc.

FDA 510(k) clearance K882634 for VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE, Substantially Equivalent on 1988-07-15. Applicant: Vistech Consultants, Inc.. Device class: 1.

Clearance details

Applicant: Vistech Consultants, Inc.
Product code: Code HOX
Device class: Class 1
Regulation: 21 CFR 886.1150
Advisory panel: Ophthalmic
Date received: 1988-06-27
Decision date: 1988-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dayton, OH, 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
K881358 — PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM1988-06-27

More clearances from Vistech Consultants, Inc.

view all

K881059 — MCT 8000 (MULTI-VISION CONTRAST TESTER)1988-04-04
K881021 — VCTS 700S SYSTEM1988-04-01
K881022 — VCTS MARKETING PROGRAM SYSTEM1988-04-01
K881023 — VCTS 6500 SYSTEM1988-04-01
K853481 — VISTECH VCTS GLARE TESTER1985-10-29

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