PMA P030054S348
- Device
- Promote+, Unify, Unify Quadra, Unify Assura, Quadra Assura, Quadra Assura MP, QuickFlex u, Quartet, Quartet (MR Conditio
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S348
- Product code
- NIK
- Decision date
- 2018-02-22
- Classification
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (crt-d)
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Approval order statement
- Adjust the relative humidity in the device and leads manufacturing and product packaging areas located in the Sylmar, California facility.
Current openFDA PMA Record#
- Device
- Promote+, Unify, Unify Quadra, Unify Assura, Quadra Assura, Quadra Assura MP, QuickFlex u, Quartet, Quartet (MR Conditio
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S348
- Product code
- NIK
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Decision date
- 2018-02-22
- Decision code
- OK30
- Date received
- 2018-01-31
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Adjust the relative humidity in the device and leads manufacturing and product packaging areas located in the Sylmar, California facility.