Disposable ureteral access sheath
K-Number: K243710 · 2025-04-11
Device Summary
Frequently Asked Questions
What is the Disposable ureteral access sheath?
Disposable ureteral access sheath is a medical device that received FDA 510(k) clearance on 2025-04-11. The listed applicant is Shenzhen Trious Medical Technology Co., Ltd.. The 510(k) number is K243710.
When did Disposable ureteral access sheath receive FDA 510(k) clearance?
Disposable ureteral access sheath received FDA 510(k) clearance on 2025-04-11, under 510(k) number K243710.
Who is the listed applicant for Disposable ureteral access sheath?
The FDA 510(k) record lists Shenzhen Trious Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Disposable ureteral access sheath?
The FDA product code for Disposable ureteral access sheath is FED.
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 Shenzhen Trious Medical Technology 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: FED)
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.