PMA P990037S005
- Device
- VASCULAR SOLUTIONS DUETT SEALING DEVICE
- Applicant
- Vascular Solutions, Inc.
- PMA number
- P990037
- Supplement
- S005
- Product code
- MGB
- Decision date
- 2001-10-31
- Classification
- Device, Hemostasis, Vascular
- Generic name
- Device, hemostasis, vascular
- Approval order statement
- APPROVAL FOR A MODIFIED CATHETER TO BE USED WITH THE DUETT MODEL 1000 SEALING DEVICE.
Current openFDA PMA Record#
- Device
- VASCULAR SOLUTIONS DUETT SEALING DEVICE
- Applicant
- Vascular Solutions, Inc.
- PMA number
- P990037
- Supplement
- S005
- Product code
- MGB
- Generic name
- Device, hemostasis, vascular
- Decision date
- 2001-10-31
- Decision code
- APPR
- Date received
- 2001-05-01
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR A MODIFIED CATHETER TO BE USED WITH THE DUETT MODEL 1000 SEALING DEVICE.