PMA P930038S026
- Device
- ANGIO-SEAL VASCULAR DEVICE - 8F AND 6F
- Applicant
- Terumo Medical Corporation
- PMA number
- P930038
- Supplement
- S026
- Product code
- MGB
- Decision date
- 2000-11-29
- Classification
- Device, Hemostasis, Vascular
- Generic name
- Device, hemostasis, vascular
- Approval order statement
- APPROVAL FOR AN ALTERNATE MANUFACTURING FACILITY LOCATED AT ST. JUDE MEDICAL, PUERTO RICO, CAGUAS, PUERTO RICO.
Current openFDA PMA Record#
- Device
- ANGIO-SEAL VASCULAR DEVICE - 8F AND 6F
- Applicant
- Terumo Medical Corporation
- PMA number
- P930038
- Supplement
- S026
- Product code
- MGB
- Generic name
- Device, hemostasis, vascular
- Decision date
- 2000-11-29
- Decision code
- APPR
- Date received
- 2000-06-27
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR AN ALTERNATE MANUFACTURING FACILITY LOCATED AT ST. JUDE MEDICAL, PUERTO RICO, CAGUAS, PUERTO RICO.