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Parker Quality & Compliance

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510(k) clearance

LithoVue Elite Digital Flexible Ureteroscope System

FDA 510(k) source

510(k) number
K261153
Applicant
Boston Scientific Corporation
Decision date
Aug 26, 2026
Date received
Apr 8, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
FGB
Device type
Ureteroscope And Accessories, Flexible/Rigid
Device class
Class II
Regulation
21 CFR 876.1500
Advisory committee
Gastroenterology, Urology
Statement or summary
Summary
Third party
N
Location
Marlborough, MA, US