FDA 510(k) Application Details - K250949

Device Classification Name	Endoscope Channel Accessory   More FDA Info for this Device
510(K) Number	K250949
Device Name	Endoscope Channel Accessory
Applicant	Olympus Medical Systems Corporation 2951 Ishikawa-cho Hachioji-shi JP Other 510(k) Applications for this Company
Contact	Osamu Tamada Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	ODC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/28/2025
Decision Date	07/16/2025
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