FDA 510(k) Application Details - K231900

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K231900
Device Name	Syringe, Piston
Applicant	Elcam Medical ACAL Kibbutz BarAm Baram 1386000 IL Other 510(k) Applications for this Company
Contact	Yaniv Menachem Other 510(k) Applications for this Contact
Regulation Number	880.5860   More FDA Info for this Regulation Number
Classification Product Code	FMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/28/2023
Decision Date	07/25/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review