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

Knife, Intraocular Pressure Lowering

21 CFR 878.4400 / General, Plastic Surgery
FDA source (opens on fda.gov)

QUQ is the FDA product code for Knife, Intraocular Pressure Lowering, a class II device type, regulated under 21 CFR 878.4400. FDA's definition for this code reads: "A knife intended for cutting of trabecular meshwork to reduce intraocular pressure in glaucoma". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
QUQ
Device name
Knife, Intraocular Pressure Lowering
FDA definition
A knife intended for cutting of trabecular meshwork to reduce intraocular pressure in glaucoma
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code QUQ

By decision year
1 clearance under product code QUQ with a decision year between 2024 and 2024, 2024 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code QUQ by decision year
YearClearances
20241

Applicants with the most clearances

Product code QUQ
Applicants holding the most 510(k) clearances under product code QUQ
ApplicantClearances
New World Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code