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

Simulatan (Including Crossed Cylinder)

21 CFR 886.1840 / Ophthalmic
FDA source (opens on fda.gov)

HOR is the FDA product code for Simulatan (Including Crossed Cylinder), a class I device type, regulated under 21 CFR 886.1840. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
HOR
Device name
Simulatan (Including Crossed Cylinder)
Regulation
21 CFR 886.1840
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
1
Ingested recalls
0

Clearances, product code HOR

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

Applicants with the most clearances

Product code HOR
Applicants holding the most 510(k) clearances under product code HOR
ApplicantClearances
Richmond Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code