PMA P030054S336
- Device
- Quadra Assura MP CRT-D, Quadra Assura CRT-D, Unify Assura CRT-D, Unify Quadra CRT-D, Promote Quadra CRT-D, Promote Q CRT
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S336
- Product code
- NIK
- Decision date
- 2017-09-11
- Classification
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (crt-d)
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Approval order statement
- Change in the header manufacturing process.
Current openFDA PMA Record#
- Device
- Quadra Assura MP CRT-D, Quadra Assura CRT-D, Unify Assura CRT-D, Unify Quadra CRT-D, Promote Quadra CRT-D, Promote Q CRT
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S336
- Product code
- NIK
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Decision date
- 2017-09-11
- Decision code
- OK30
- Date received
- 2017-08-16
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Change in the header manufacturing process.