FDA 510(k) Application Details - K240374

Device Classification Name	Ureteroscope And Accessories, Flexible/Rigid   More FDA Info for this Device
510(K) Number	K240374
Device Name	Ureteroscope And Accessories, Flexible/Rigid
Applicant	Shenzhen HugeMed Medical Technical Development Co., Ltd. 401, 501, Building 4, Haizhi Technology Park, Fortis, No.17 Bulan Rd.,Xialilang Community, Nanwan St., Longgang District Shenzhen 518115 CN Other 510(k) Applications for this Company
Contact	Cathy Shi Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FGB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/07/2024
Decision Date	05/10/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review