FDA 510(k) Application Details - K221702

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K221702
Device Name	Syringe, Piston
Applicant	Milestone Scientific, Inc. 425 Eagle Rock Ave Suite 403 Roseland, NJ 07068 US Other 510(k) Applications for this Company
Contact	Arjan Haverhals 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	06/13/2022
Decision Date	02/25/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review