FDA 510(k) Application Details - K170900

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K170900
Device Name	Syringe, Piston
Applicant	INTERVENE Group Ltd Russell Building, Brunel Science Park, Kingston Lane Uxbridge UB8 3PQ GB Other 510(k) Applications for this Company
Contact	Homer Trieu 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	03/27/2017
Decision Date	11/09/2017
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