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

Grid, Amsler

21 CFR 886.1330 / Ophthalmic
FDA source (opens on fda.gov)

HOQ is the FDA product code for Grid, Amsler, a class I device type, regulated under 21 CFR 886.1330. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HOQ
Device name
Grid, Amsler
Regulation
21 CFR 886.1330
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
8
Ingested recalls
0

Clearances, product code HOQ

By decision year
8 clearances under product code HOQ with a decision year between 1985 and 2018, 1985 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code HOQ by decision year
YearClearances
19852
19871
19881
20021
20131
20151
20181

Applicants with the most clearances

Product code HOQ
Applicants holding the most 510(k) clearances under product code HOQ
ApplicantClearances
Vital Art and Science Incorporated2
Wheel Checkers2
Danek Medical, Inc.1
Notal Vision Ltd.1
Oculocare Medical AG1
Richmond Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code