510(k) K160252

OmniPod Insulin Management System by Insulet Corporation — Product Code LZG

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 27, 2016
Date Received
February 1, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Infusion, Insulin
Device Class
Class II
Regulation Number
880.5725
Review Panel
CH
Submission Type