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

Single-Use Flexible Ureteroscope

K Number: K230200 · Decision May 18, 2023
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
112
Applicant Total
17
Review Days
113

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Basic Information

Device Name
Single-Use Flexible Ureteroscope
K Number
K230200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hunan Vathin Medical Instrument Co., Ltd.
Date Received
January 25, 2023
Decision Date
May 18, 2023
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FGB), ordered by most recent decision date.

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Other Clearances by Hunan Vathin Medical Instrument Co., Ltd.

K Number Device Name
K250232 Vathin® Video Bronchoscope System
K251599 Single-use Ureteral Access Sheath
K250785 Single-use Flexible Ureteroscope
K243117 Digital Video Processor
K242416 Single-use Flexible Bronchoscope: BC-E1C10, BC-E1C11, BC-E1C12, BC-E1E10, BC-E1E11, BC-E1E12, BC-E1H10, BC-E1H11, BC-E1H12; Digital Video Monitor: DVM-D1, DVM-D2; Single-use sampler: S-20mL, S-30mL, S-50mL
K242535 Single-use Flexible Cystoscope (CY-E2E01, CY-E2E01R, CY-E2F01, CY-E2F01R, CY-E2G01, CY-E2G01R, CY-S2E01, CY-S2E01R); Digital Video Monitor (DVM-D1, DVM-D2)
K241612 Video Bronchoscope System; Single-use Flexible Bronchoscope (BC-S1E00-L, BC-S1H00-L, BC-S1J00-L, BC-S1E00, BC-S1H00, BC-S1J00.); Digital Video Monitor (DVM-D1, DVM-D2)
K240167 Single-use Ureteral Access Sheath
K241434 Video Ureteroscope System
K231135 Video Ureteroscope System
Search all 17 clearances from Hunan Vathin Medical Instrument Co., Ltd. →