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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

Single-use Digital Flexible Ureteroscope (GY-UR6.3); Single-use Digital Flexible Ureteroscope (GY-UR6.3A)

FDA 510(k) source

510(k) number
K262437
Applicant
Zhejiang Geyi Medical Instrument Co., Ltd.
Decision date
Oct 29, 2026
Date received
Jul 16, 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
Jiande City, CN