PMA P030054S357

Device
QuickFlex u and Quartet
Applicant
ABBOTT MEDICAL
PMA number
P030054
Supplement
S357
Product code
NIK
Decision date
2018-07-19
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 the cleaning agent and cleaning process on the incoming tools used in the manufacture of MCRDs.

Current openFDA PMA Record#

Device
QuickFlex u and Quartet
Applicant
ABBOTT MEDICAL
PMA number
P030054
Supplement
S357
Product code
NIK
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Decision date
2018-07-19
Decision code
OK30
Date received
2018-07-02
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Change the cleaning agent and cleaning process on the incoming tools used in the manufacture of MCRDs.