FDA 510(k) Application Details - K232327

Device Classification Name	Endoscope Channel Accessory   More FDA Info for this Device
510(K) Number	K232327
Device Name	Endoscope Channel Accessory
Applicant	Endostart s.r.l. Via delle Regioni 265 Certaldo 50052 IT Other 510(k) Applications for this Company
Contact	Alessandro Tozzi 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	08/03/2023
Decision Date	03/15/2024
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