FDA 510(k) Application Details - K203738

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K203738
Device Name	Syringe, Piston
Applicant	Medex 240 allΘe Jacques Monod Saint-Priest 69800 FR Other 510(k) Applications for this Company
Contact	Sandra Thiolliere 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	12/22/2020
Decision Date	03/14/2022
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