PMA P930038S078
- Device
- ANGIO-SEAL
- Applicant
- Terumo Medical Corporation
- PMA number
- P930038
- Supplement
- S078
- Product code
- MGB
- Decision date
- 2015-09-30
- Classification
- Device, Hemostasis, Vascular
- Generic name
- Device, hemostasis, vascular
- Approval order statement
- APPROVAL FOR IMPLEMENTATION OF A SUTURE KNOT TEST INSPECTION.
Current openFDA PMA Record#
- Device
- ANGIO-SEAL
- Applicant
- Terumo Medical Corporation
- PMA number
- P930038
- Supplement
- S078
- Product code
- MGB
- Generic name
- Device, hemostasis, vascular
- Decision date
- 2015-09-30
- Decision code
- APPR
- Date received
- 2015-09-04
- Supplement type
- Special (Immediate Track)
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR IMPLEMENTATION OF A SUTURE KNOT TEST INSPECTION.