FDA 510(k) Application Details - K233031

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K233031
Device Name	Instrument, Biopsy
Applicant	Canyon Medical Inc. Building 3, Phase 2 Accelerator, No. 11 Yaogu Avenue, Jiangbei New Area, Jiangsu Province Nanjing 210032 CN Other 510(k) Applications for this Company
Contact	Jin Mingzhi Other 510(k) Applications for this Contact
Regulation Number	876.1075   More FDA Info for this Regulation Number
Classification Product Code	KNW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/25/2023
Decision Date	01/17/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review