PMA P020024S049
- Device
- AMPLATZER Duct Occluder
- Applicant
- ABBOTT MEDICAL
- PMA number
- P020024
- Supplement
- S049
- Product code
- MAE
- Decision date
- 2017-08-03
- Classification
- Occluder, Patent Ductus, Arteriosus
- Generic name
- OCCLUDER, PATENT DUCTUS, ARTERIOSUS
- Approval order statement
- Change to laser parameters on the laser used to weld the occluder braid.
Current openFDA PMA Record#
- Device
- AMPLATZER Duct Occluder
- Applicant
- ABBOTT MEDICAL
- PMA number
- P020024
- Supplement
- S049
- Product code
- MAE
- Generic name
- OCCLUDER, PATENT DUCTUS, ARTERIOSUS
- Decision date
- 2017-08-03
- Decision code
- OK30
- Date received
- 2017-07-06
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Change to laser parameters on the laser used to weld the occluder braid.