PMA P990037S022
- Device
- DUETT PRO SEALING DEVICE MODEL 1010
- Applicant
- Vascular Solutions, Inc.
- PMA number
- P990037
- Supplement
- S022
- Product code
- MGB
- Decision date
- 2004-07-09
- Classification
- Device, Hemostasis, Vascular
- Generic name
- Device, hemostasis, vascular
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT STERIS CORP., ISOMEDIX SERVICES, MINNEAPOLIS, MINNESOTA.
Current openFDA PMA Record#
- Device
- DUETT PRO SEALING DEVICE MODEL 1010
- Applicant
- Vascular Solutions, Inc.
- PMA number
- P990037
- Supplement
- S022
- Product code
- MGB
- Generic name
- Device, hemostasis, vascular
- Decision date
- 2004-07-09
- Decision code
- APPR
- Date received
- 2004-06-15
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT STERIS CORP., ISOMEDIX SERVICES, MINNEAPOLIS, MINNESOTA.