PMA P100013S009
- Device
- EXOSEAL VASCULAR CLOSURE DEVICE
- Applicant
- Cordis US Corporation
- PMA number
- P100013
- Supplement
- S009
- Product code
- MGB
- Decision date
- 2013-05-09
- Classification
- Device, Hemostasis, Vascular
- Generic name
- Device, hemostasis, vascular
- Approval order statement
- CHANGE IN THE PROCESSING OF THREE COMPONENTS FROM SINGLE CAVITYMOLD TO MULTI CAVITY MOLDS FOR THE EXOSEAL VASCULAR CLOSURE DEVICE.
Current openFDA PMA Record#
- Device
- EXOSEAL VASCULAR CLOSURE DEVICE
- Applicant
- Cordis US Corporation
- PMA number
- P100013
- Supplement
- S009
- Product code
- MGB
- Generic name
- Device, hemostasis, vascular
- Decision date
- 2013-05-09
- Decision code
- OK30
- Date received
- 2013-04-09
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE IN THE PROCESSING OF THREE COMPONENTS FROM SINGLE CAVITYMOLD TO MULTI CAVITY MOLDS FOR THE EXOSEAL VASCULAR CLOSURE DEVICE.