510(k) K111924
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 10, 2012
- Date Received
- July 6, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pump, Infusion, Insulin Bolus
- Device Class
- Class II
- Regulation Number
- 880.5725
- Review Panel
- CH
- Submission Type
The device is adhered to the body for several days for the purpose of periodically infusing an insulin bolus.