PMA P030054S085
- Device
- EPIC HF/ATLAS+ HF FAMILY OF CRT-DS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S085
- Product code
- NIK
- Decision date
- 2008-04-29
- 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 A MINOR SOFTWARE UPDATE TO THE MERLIN PATIENT CARE SYSTEM (VERSION 6.6.1) AND TO THE PROGRAMMER (VERSION 6.6.1).
Current openFDA PMA Record#
- Device
- EPIC HF/ATLAS+ HF FAMILY OF CRT-DS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S085
- Product code
- NIK
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Decision date
- 2008-04-29
- Decision code
- APPR
- Date received
- 2008-03-25
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR A MINOR SOFTWARE UPDATE TO THE MERLIN PATIENT CARE SYSTEM (VERSION 6.6.1) AND TO THE PROGRAMMER (VERSION 6.6.1).