Paradise Ultrasound Renal Denervation System (Paradise System), Paradise Cartridge
FDA premarket approval P220023/S001 · decided 2023-12-06
Approval details
- PMA number
- P220023
- Supplement
- S001
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Paradise Ultrasound Renal Denervation System (Paradise System), Paradise Cartridge
- Generic name
- Ablation catheter, renal denervation
- Applicant
- Recor Medical, Inc.
- Date received
- 2023-11-20
- Decision date
- 2023-12-06
- Days to decision
- 16 days
- Decision code
- OK30
- Product code
- QYI
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Palo Alto, CA
- Statement
- modification of the cartridge packaging tray
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