The following data is part of a premarket notification filed by Insulet Corporation with the FDA for Freestyle Glucose Meter Incorporated Into The Omnipod Insulin Management Systems.
Device ID | K111669 |
510k Number | K111669 |
Device Name: | FREESTYLE GLUCOSE METER INCORPORATED INTO THE OMNIPOD INSULIN MANAGEMENT SYSTEMS |
Classification | Pump, Infusion, Insulin |
Applicant | INSULET CORPORATION 9 OAK PARK DR. Bedford, MA 01730 |
Contact | Susan Finneran |
Correspondent | Susan Finneran INSULET CORPORATION 9 OAK PARK DR. Bedford, MA 01730 |
Product Code | LZG |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-06-15 |
Decision Date | 2011-12-15 |
Summary: | summary |