FDA 510(k) Application Details - K203674

Device Classification Name	Set, I.V. Fluid Transfer   More FDA Info for this Device
510(K) Number	K203674
Device Name	Set, I.V. Fluid Transfer
Applicant	AEA srl Via Fiume 16 Angeli de Rosora 60030 IT Other 510(k) Applications for this Company
Contact	Michele Mengoni Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	LHI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/16/2020
Decision Date	09/27/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review