FDA 510(k), K191923, EverLift Submucosal Lifting Agent

510(K) Number: K191923
Device Name: EverLift Submucosal Lifting Agent
Manufacturer: GI Supply
Device Classification Name: Submucosal Injection Agent
Regulation Number: 876.1500
Classification Product Code: PLL
Date Received: 07/18/2019
Decision Date: 06/20/2020
Regulation Medical Specialty: Gastroenterology/Urology

324 pages (2,697 of 3,021 original pages are fully redacted)