510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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HOXClass I

Chart, Visual Acuity

21 CFR 886.1150 / Ophthalmic
FDA source (opens on fda.gov)

HOX is the FDA product code for Chart, Visual Acuity, a class I device type, regulated under 21 CFR 886.1150. As of , FDA records hold 32 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HOX
Device name
Chart, Visual Acuity
Regulation
21 CFR 886.1150
Device class
Class I
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
32
Ingested recalls
0

Clearances, product code HOX

By decision year
32 clearances under product code HOX with a decision year between 1978 and 2010, 1988 the highest year at 11.
Show the numbers
510(k) clearances under FDA product code HOX by decision year
YearClearances
19781
19791
19811
19823
19831
19844
19853
19863
19872
198811
19951
20101

Applicants with the most clearances

Product code HOX
Applicants holding the most 510(k) clearances under product code HOX
ApplicantClearances
Vistech Consultants, Inc.7
Mentor O & O, Inc.3
Richmond Products, Inc.2
Stereo Optical Company LLC2
Abco Dealers, Inc.1
American Ergo Systems1
Applied Vision Concepts, Inc.1
Canon Medical Components U.S.A., Inc.1
Cerenovus, Inc.1
CooperVision, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 106 companies shown, in name order