- Device
- DUETT PRO SEALING DEVICE (MODEL 1010) AND DIAGNOSTIC DUETT PRO SEALING DEVICE (MODEL 2210)
- Applicant
- Vascular Solutions, Inc.
- PMA number
- P990037
- Supplement
- S015
- Product code
- MGB
- Generic name
- Device, hemostasis, vascular
- Decision date
- 2003-05-20
- Decision code
- APPR
- Date received
- 2003-03-11
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR A DESIGN CHANGE TO THE DEUTT PRO SEALING DEVICE AND THE DIAGNOSTIC DUETT PRO SEALING DEVICE.