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

Fluid, Intraocular

21 CFR 886.4275 / Ophthalmic
FDA source (opens on fda.gov)

LWL is the FDA product code for Fluid, Intraocular, a class III device type, regulated under 21 CFR 886.4275. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LWL
Device name
Fluid, Intraocular
Regulation
21 CFR 886.4275
Device class
Class III
Review panel
Ophthalmic
Submission type
PMA
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code LWL

By decision year
1 clearance under product code LWL with a decision year between 1985 and 1985, 1985 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LWL by decision year
YearClearances
19851

Applicants with the most clearances

Product code LWL
Applicants holding the most 510(k) clearances under product code LWL
ApplicantClearances
Optical Micro Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code