FDA 510(k) Application Details - K162296

Device Classification Name	Pump, Infusion, Insulin   More FDA Info for this Device
510(K) Number	K162296
Device Name	Pump, Infusion, Insulin
Applicant	INSULET CORPORATION 600 TECHNOLOGY PARK DRIVE SUITE 200 BILLERICA, MA 01821 US Other 510(k) Applications for this Company
Contact	MATTHEW KING Other 510(k) Applications for this Contact
Regulation Number	880.5725   More FDA Info for this Regulation Number
Classification Product Code	LZG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/16/2016
Decision Date	04/18/2017
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