510(k) clearances

Single Use Ureteral Access Sheath

Zhejiang Chuangxiang Medical Technology Co., Ltd. · Gastroenterology, Urology

K260410Substantially EquivalentSpecialFED
Open FDA's page for this record
Third party flag
N
City
Hangzhou
Advisory committee description
Gastroenterology, Urology
Address 1
Rm. 101-1, 201-1, 301, 401, Bldg. 50, #650 Hongfeng Rd.
Address 2
Donghu St., Linping District
Statement or summary
Summary
Product code
FED
Zip code
311100
Applicant
Zhejiang Chuangxiang Medical Technology Co., Ltd.
Decision date
2026-09-11
Decision code
SESE
Country code
CN
Device name
Single Use Ureteral Access Sheath
Advisory committee
GU
Contact
Haishao Wei
K number
K260410
Date received
2026-02-09
Review advisory committee
GU
Postal code
311100
Decision description
Substantially Equivalent
Clearance type
Special
Harmonized identifiers (openFDA)
Device name
Endoscopic Access Overtube, Gastroenterology-Urology
Medical specialty description
Gastroenterology, Urology
Regulation number
876.1500
Device class
2
Registration number
3005814162, 8043903, 3045323889, 3021023752, 3014683069, 3013247477, 3005580113, 3032959393, 2431166, 1000121056, 3012797688, 2029275, 3014644276, 1820334, 3010421104, 1647149, 3030733800, 2936485, 3015309643, 3004361445, 9610773, 3030446844, 3042172882, 3002808148, 3009420598, 3016881508, 9611668, 1037955, 3034608931, 8043746, 1018233, 3013944123, 3005941719, 3010273872, 3033589330, 3015225571, 3011050570, 1724474, 1000393132, 3044858680 +77 more
FEI number
3005814162, 3045323889, 3021023752, 3014683069, 3013247477, 3005580113, 3032959393, 3003995201, 1000514656, 1000121056, 3012797688, 1820334, 3010421104, 1000136543, 3030733800, 1000120613, 2936485, 3015309643, 3004361445, 3006149253, 1000122656, 3002807135, 1000160215, 3030446844, 3042172882, 3002806565, 3002808148, 3009420598, 3016881508, 1037955, 3034608931, 1018233, 3013944123, 3002807795, 3002808088, 3010273872, 3033589330, 3015225571, 3002808127, 3011050570 +77 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.