Video Ureteroscope System
K-Number: K241434 · 2024-10-04
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Device Summary
Frequently Asked Questions
What is the Video Ureteroscope System?
Video Ureteroscope System is a medical device that received FDA 510(k) clearance on 2024-10-04. The listed applicant is Hunan Vathin Medical Instrument Co., Ltd.. The 510(k) number is K241434.
When did Video Ureteroscope System receive FDA 510(k) clearance?
Video Ureteroscope System received FDA 510(k) clearance on 2024-10-04, under 510(k) number K241434.
Who is the listed applicant for Video Ureteroscope System?
The FDA 510(k) record lists Hunan Vathin Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Video Ureteroscope System?
The FDA product code for Video Ureteroscope System is FGB.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Hunan Vathin Medical Instrument Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FGB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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