FDA 510(k) Application Details - K241842

Device Classification Name	Endoscope Channel Accessory   More FDA Info for this Device
510(K) Number	K241842
Device Name	Endoscope Channel Accessory
Applicant	Olympus Medical Systems Corporation 2951 Ishikawa-cho Hachioji-shi 192-8507 JP Other 510(k) Applications for this Company
Contact	Shinichiro Kawachi 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	06/26/2024
Decision Date	03/19/2025
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