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

Applicator, Ocular Pressure

21 CFR 886.4610 / Ophthalmic
FDA source (opens on fda.gov)

LCC is the FDA product code for Applicator, Ocular Pressure, a class II device type, regulated under 21 CFR 886.4610. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LCC
Device name
Applicator, Ocular Pressure
Regulation
21 CFR 886.4610
Device class
Class II
Review panel
Ophthalmic
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
6
Ingested recalls
0

Clearances, product code LCC

By decision year
6 clearances under product code LCC with a decision year between 1979 and 2012, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LCC by decision year
YearClearances
19791
19821
19841
19851
19951
20121

Applicants with the most clearances

Product code LCC
Applicants holding the most 510(k) clearances under product code LCC
ApplicantClearances
Keeler Optical Products, Ltd.1
MicroSurgical Technology Inc1
Oryx Medical Pty, Ltd.1
Surgi-Quip Inc.U1
The Lebanon Corp.1
Visitec Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code