Cleared Traditional

MCB UNIT Model: V10GMCBUS

K222542 · Lamidey Noury Medical · Gastroenterology & Urology
Sep 2022
Decision
30d
Days
Class 2
Risk

About This 510(k) Submission

K222542 is an FDA 510(k) clearance for the MCB UNIT Model: V10GMCBUS, a Unit, Electrosurgical, Endoscopic (with Or Without Accessories) (Class II — Special Controls, product code KNS), submitted by Lamidey Noury Medical (Verriere Le Buisson, FR). The FDA issued a Cleared decision on September 21, 2022, 30 days after receiving the submission on August 22, 2022. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.4300.

Submission Details

510(k) Number K222542 FDA.gov
FDA Decision Cleared SESE
Date Received August 22, 2022
Decision Date September 21, 2022
Days to Decision 30 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code KNS — Unit, Electrosurgical, Endoscopic (with Or Without Accessories)
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.4300

Similar Devices — KNS Unit, Electrosurgical, Endoscopic (with Or Without Accessories)

All 186
Vanquish Water Vapor Ablation Device
K252388 · Francis Medical, Inc. · Nov 2025
Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M)
K252889 · Olympus Medical Systems Corporation · Nov 2025
Single Use Preloaded Sphincterotome V (Distal Wire Guided) (KD-VC600 Series); Single Use Sphincterotome V (Distal Wire Guided) (KD-VC400 Series); Single Use 3-Lumen Sphincterotome (KD-V Series); Disposable Triple Lumen Sphincterotome (KD Series)
K250945 · Olympus Medical Systems Corp. · Oct 2025
Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife (KD-620UR); Single Use Electrosurgical Knife (KD-650L, KD-650U)
K250351 · Olympus Medical Systems Corporation · Oct 2025
SureTome? SW Sphincterotome with DomeTip
K251104 · Wilson Cook Medical · Sep 2025
Aqua Medical RF Vapor Ablation System
K251226 · Aqua Medical, Inc. · Aug 2025