PMA P230021S001
- Device
- Duo Venous Stent System
- Applicant
- Philips Image Guided Therapy Corporation
- PMA number
- P230021
- Supplement
- S001
- Product code
- QAN
- Decision date
- 2025-02-11
- Classification
- Cardiovascular
- Generic name
- Stent, iliac vein
- Approval order statement
- a change to the Vesper Medical operating location
Current openFDA PMA Record#
- Device
- Duo Venous Stent System
- Applicant
- Philips Image Guided Therapy Corporation
- PMA number
- P230021
- Supplement
- S001
- Product code
- QAN
- Generic name
- Stent, iliac vein
- Decision date
- 2025-02-11
- Decision code
- OK30
- Date received
- 2025-01-13
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- a change to the Vesper Medical operating location