MENTOR POTENTIAL ACUITY METER— 510(k) K821932

Name: FDA 510(k) clearance K821932
Creator: U.S. Food and Drug Administration
Published: 1982-08-03

Substantially Equivalent

Mentor O & O, Inc.

FDA 510(k) clearance K821932 for MENTOR POTENTIAL ACUITY METER, Substantially Equivalent on 1982-08-03. Applicant: Mentor O & O, Inc.. Device class: 1.

Clearance details

Applicant: Mentor O & O, Inc.
Product code: Code HOX
Device class: Class 1
Regulation: 21 CFR 886.1150
Advisory panel: Ophthalmic
Date received: 1982-06-29
Decision date: 1982-08-03
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

More clearances from Mentor O & O, Inc.

view all

K955245 — MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEM1996-02-12
K934320 — MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATION1994-02-16
K912904 — MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEM1992-06-11
K915340 — MENTOR HORIZON LOW VISION MAGNIFIER1992-03-30
K910637 — MENTOR(R) SUR-E-TROL(R)1991-05-13

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