Class Class II

Single-use Ureteral Access Sheath (K250695)

K250695 2025-07-08 Traditional
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Description

Single-use Ureteral Access Sheath by Shenzhen HugeMed Medical Technical Development Co., Ltd., an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250695
Clearance Date2025-07-08
Clearance TypeTraditional
Product CodeFED
Regulation Number876.1500

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Predicate lineage for K250695

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Single-use Ureteral Access Sheath (K250695) cites 1 predicate device and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K241181Disposable Ureteral Guide SheathDongguan Zsr Biomedical Technology ...2024

Trace the full predicate network for K250695

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

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