QUQ

Knife, Intraocular Pressure Lowering

Product code
QUQ
Device name
Knife, Intraocular Pressure Lowering
Device class
Class 2
21 CFR
21 CFR 878.4400
Medical specialty
General, Plastic Surgery
Marketing pathway
510(K)
510(k) clearances (last 3 years)
1

FDA classification definition

A knife intended for cutting of trabecular meshwork to reduce intraocular pressure in glaucoma

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2024-05-17.

NumberDecision dateApplicantDevice nameSummary
K2208912024-05-17New World Medical, Inc.Kahook Dual Blade Glide (KDB Glide)PDF

1 summaries are archived here for direct download.

Official FDA classification page: QUQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).