PMA P030054S082
- Device
- EPIC HF FAMILY OF CRT-DS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S082
- Product code
- NIK
- Decision date
- 2008-03-11
- 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 ADDITION OF A MANUFACTURING INSPECTION STEP TO VERIFY BATTERY PIN PLACEMENT.
Current openFDA PMA Record#
- Device
- EPIC HF FAMILY OF CRT-DS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S082
- Product code
- NIK
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Decision date
- 2008-03-11
- Decision code
- APPR
- Date received
- 2008-02-12
- Supplement type
- Special (Immediate Track)
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR THE ADDITION OF A MANUFACTURING INSPECTION STEP TO VERIFY BATTERY PIN PLACEMENT.