FDA 510(k) Application Details - K243618

Device Classification Name	System, Perfusion, Kidney   More FDA Info for this Device
510(K) Number	K243618
Device Name	System, Perfusion, Kidney
Applicant	Bridge to Life 707 Skokie Boulevard, Suite 340 Northbrook, IL 60062 US Other 510(k) Applications for this Company
Contact	Mark Harper Other 510(k) Applications for this Contact
Regulation Number	876.5880   More FDA Info for this Regulation Number
Classification Product Code	KDN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/22/2024
Decision Date	06/17/2025
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