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

Screen, Tangent, Target

21 CFR 886.1810 / Ophthalmic
FDA source (opens on fda.gov)

HOJ is the FDA product code for Screen, Tangent, Target, a class I device type, regulated under 21 CFR 886.1810. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HOJ
Device name
Screen, Tangent, Target
Regulation
21 CFR 886.1810
Device class
Class I
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code HOJ

By decision year
3 clearances under product code HOJ with a decision year between 1982 and 1987, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HOJ by decision year
YearClearances
19821
19841
19871

Applicants with the most clearances

Product code HOJ
Applicants holding the most 510(k) clearances under product code HOJ
ApplicantClearances
Medical Equipment Designs, Inc.1
Pro Design Intl. AS1
Richmond Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code