Single-Use Flexible Ureteroscope— 510(k) K230200
Substantially EquivalentHunan Vathin Medical Instrument Co., Ltd.
FDA 510(k) clearance K230200 for Single-Use Flexible Ureteroscope, Substantially Equivalent on 2023-05-18. Applicant: Hunan Vathin Medical Instrument Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Hunan Vathin Medical Instrument Co., Ltd.
- Product code
- Code FGB
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Xingtan, CN
Recent devices under product code FGB
view all- K262488 — Single-Use Video Flexible Ureterorenoscope (RP-U-C06R9, RP-U-C06R3, RP-U-C06S9, RP-U-C06S3)
- K261153 — LithoVue Elite Digital Flexible Ureteroscope System
- K262552 — Single-use Flexible Ureteroscope (Single-use Flexible Ureteroscope: SUV-5C-B)
- K253505 — Zamenix P
- K260516 — BubbleView Single-Use Digital Flexible Cystoscope (C38-CS, C38-CRS, C50-C, C50-CR, C50-CB, C50-CBR)
More clearances from Hunan Vathin Medical Instrument Co., Ltd.
view all- 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 +2 more
Adverse events under product code FGB
product code FGB- Death
- 6
- Injury
- 552
- Malfunction
- 3,922
- Other
- 1
- Total
- 4,481
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.