QUQ — Knife, Intraocular Pressure Lowering Class II

FDA Device Classification

FDA product code QUQ covers "Knife, Intraocular Pressure Lowering", a Class II medical device regulated under 21 CFR 878.4400. Submissions are reviewed by the General, Plastic Surgery panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
QUQ
Device Class
Class II
Regulation Number
878.4400
Submission Type
Review Panel
OP
Medical Specialty
General, Plastic Surgery
Implant
No

Definition

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K220891new world medicalKahook Dual Blade Glide (KDB Glide)May 17, 2024