MINIMED 530G INSULIN PUMP
FDA premarket approval P120010/S076 · decided 2016-06-03
Approval details
- PMA number
- P120010
- Supplement
- S076
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- MINIMED 530G INSULIN PUMP
- Generic name
- Automated insulin dosing , threshold suspend
- Applicant
- Medtronic, Inc.
- Date received
- 2015-11-03
- Decision date
- 2016-06-03
- Days to decision
- 213 days
- Decision code
- APPR
- Product code
- OZO
- Advisory committee
- Clinical Chemistry
- Expedited review
- No
- Location
- Northridge, CA
- Statement
- Approval for changes to the pump case drive support cap assembly process and the automated adhesive dispensing process used in the pump case manufacturing process of the Paradigm family of insulin pumps (models 5xx and 7xx). Paradigm insulin pumps are components of the Paradigm REAL-Time System, Paradigm REAL-Time Revel System and the MiniMed 530G System.
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