PMA P030054S127
- Device
- EPIC HF/EPIC+ HF/EPIC II HF/EPIC II+HF/ATLAS HF/ATLAS+HF/ATLAS II HF/ATLAS II+HF CRT-DS/QUICKSITE/QUICKFLEX LEADS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S127
- Product code
- NIK
- Decision date
- 2009-07-10
- Classification
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (crt-d)
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Approval order statement
- THREE STERILIZATION CHANGES.
Current openFDA PMA Record#
- Device
- EPIC HF/EPIC+ HF/EPIC II HF/EPIC II+HF/ATLAS HF/ATLAS+HF/ATLAS II HF/ATLAS II+HF CRT-DS/QUICKSITE/QUICKFLEX LEADS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S127
- Product code
- NIK
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Decision date
- 2009-07-10
- Decision code
- OK30
- Date received
- 2009-06-10
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- THREE STERILIZATION CHANGES.