PMA P030054S113
- Device
- EPIC HF/ATLAS + HF FAMILY OF CRT-DS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S113
- Product code
- NIK
- Decision date
- 2009-02-04
- Classification
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (crt-d)
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Approval order statement
- APPROVAL FOR THE CURRENT+ ICDS AND PROMOTE+ CRT-DS.
Current openFDA PMA Record#
- Device
- EPIC HF/ATLAS + HF FAMILY OF CRT-DS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S113
- Product code
- NIK
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Decision date
- 2009-02-04
- Decision code
- APPR
- Date received
- 2009-01-02
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR THE CURRENT+ ICDS AND PROMOTE+ CRT-DS.