Product code HOX— Ophthalmic
'E' CUBE AND 'E' PAD
- Classification name
- Chart, Visual Acuity
- Device class
- Class 1
- Regulation
- 21 CFR 886.1150
- Advisory panel
- Ophthalmic
- Total cleared
- 32
- First cleared
- Most recent
Market context for product code HOX
FDA has cleared devices under product code HOX between 1978 and 2010, filed by 22 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 2010
- 1995
- 1988
- 1987
- 1986
- 1985
- 1984
- 1983
- 1982
- 1981
- 1979
- 1978
Top applicants under product code HOX
Recent clearances under product code HOX
- K100095 — CENTRAL VISION ANALYZER MODEL 1000
- K944156 — HEINE LAMBDA 100
- K881971 — OCCU-TECH VISION TEST
- K883337 — PL 20/20 INFANT VISION TESTER
- K882634 — VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE
- K881358 — PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM
- K881059 — MCT 8000 (MULTI-VISION CONTRAST TESTER)
- K880647 — ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)
- K881021 — VCTS 700S SYSTEM
- K881022 — VCTS MARKETING PROGRAM SYSTEM
- K881023 — VCTS 6500 SYSTEM
- K875237 — OPTEC 1000 DMV VISION TESTER MODIFY
- K875112 — MENTOR B-VAT(TM) II VIDEO TESTER
- K873916 — 'E' CUBE AND 'E' PAD
- K873909 — READING CHARTS-CARDS (DISTANCE AND NEARPOINT)
- K863509 — OPTEC 1000 DMV
- K861416 — CANON AUTO ACUITOMETER CV-10
- K854983 — OPTRONICS CONTRAST ACUITY TESTER
- K854047 — IN-HOME VISION MONITORING KIT
- K853736 — MENTOR BRIGHTNESS ACUITY TESTER
- K853481 — VISTECH VCTS GLARE TESTER
- K840255 — VISTECH VCTS 6000
- K834145 — ERGO DIAGNOSTIC CARD
- K833778 — TESTING VISUAL ACUITY
- K833956 — DOT VISUAL ACVITY TEST 2000
- K830011 — VFS 1000/SCREENING FUNCTION ANALYZER
- K822215 — NIC OPTRONICS CS-2000
- K821932 — MENTOR POTENTIAL ACUITY METER
- K813376 — EYE CHARTS
- K803256 — EYETECH-VISION SCREENING SYSTEM
- K790909 — OPHTHALMIC DRESSING TRAY
- K781452 — BAYLOW VISUAL ACUITY TESTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.