Prometra Programmable Infusion Pump System
FDA premarket approval P080012/S043 · decided 2017-06-07
Approval details
- PMA number
- P080012
- Supplement
- S043
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Prometra Programmable Infusion Pump System
- Generic name
- Pump, infusion, implanted, programmable
- Applicant
- Infusyn Therapeutics, LLC
- Date received
- 2017-05-10
- Decision date
- 2017-06-07
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- LKK
- Advisory committee
- General Hospital
- Expedited review
- No
- Location
- Hackettstown, NJ
- Statement
- Alternate supplier (Hudson Technologies Company, One Blue Hill Plaza, Pearl River, New York) of R-21(dichlorofluoromethane) for the Prometra Programmable Infusion Pump System.
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