FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Single use flexible ureteroscope (UR-D1); Single use flexible ureteroscope (UR-D2); Single use flexible ureteroscope (UR-F1); Single use flexible ureteroscope (UR-F2)

K Number: K240074 · Decision Oct 4, 2024
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
112
Applicant Total
1
Review Days
268

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Basic Information

Device Name
Single use flexible ureteroscope (UR-D1); Single use flexible ureteroscope (UR-D2); Single use flexible ureteroscope (UR-F1); Single use flexible ureteroscope (UR-F2)
K Number
K240074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shenzhen Besdata Technology Co., Ltd.
Date Received
January 10, 2024
Decision Date
October 4, 2024
Product Code
FGB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FGB Ureteroscope And Accessories, Flexible/Rigid

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