FDA 510(k) Application Details - K202652

Device Classification Name	System, Perfusion, Kidney   More FDA Info for this Device
510(K) Number	K202652
Device Name	System, Perfusion, Kidney
Applicant	S.A.L.F. spa Via Marconi 2 Cenate Sotto 24069 IT Other 510(k) Applications for this Company
Contact	Carmelo Gagliano 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	09/14/2020
Decision Date	08/19/2021
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