FDA 510(k) Application Details - K223354

Device Classification Name	Catheter, Biliary, Diagnostic   More FDA Info for this Device
510(K) Number	K223354
Device Name	Catheter, Biliary, Diagnostic
Applicant	S&G Biotech Inc. 82, Bugok-ro, Pogok-eup, Cheoin-gu, Yongin-si 17023 KR Other 510(k) Applications for this Company
Contact	Sung-Kwon Kang Other 510(k) Applications for this Contact
Regulation Number	876.5010   More FDA Info for this Regulation Number
Classification Product Code	FGE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/02/2022
Decision Date	09/21/2023
Decision	SESU - SE - WITH LIMITATIONS
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