FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Automated Insulin Dosing , Threshold Suspend
PMA: P150001
·
Supplement: S014
·
Decision May 10, 2017
Classifications
1
FEI Numbers
18
Registration Numbers
18
Basic Information
- Device Name
- Automated Insulin Dosing , Threshold Suspend
- Trade Name
- MiniMed 630G Insulin Pump
- PMA Number
- P150001
- Supplement Number
- S014
- Device Class
- FDA Class 3
- Product Code
- OZO
- Generic Name
- Automated insulin dosing , threshold suspend
- Medical Specialty
- Unknown
- Advisory Committee
- Clinical Chemistry
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- May 10, 2017
- Date Received
- April 10, 2017
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Transfer equipment used for leak testing seals of the Paradigm insulin infusion pumps and Next Generation insulin infusion pumps from Medtronic MiniMed to a sub-tier supplier, as well as transferring the task of performing such testing to the sub-tier supplier. The Paradigm insulin infusion pump is component of the Paradigm REAL-Time System, the Paradigm REAL-Time Revel System, and the MiniMed 530G System. The Next Generation insulin infusion pump is a component of the MiniMed 630G System and the MiniMed 670G System.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| OZO | Automated Insulin Dosing , Threshold Suspend | FDA class 3 | Unknown |