PMA P030052S018

Device
UROVYSION BLADDER CANCER KIT
Applicant
Abbott Molecular
PMA number
P030052
Supplement
S018
Decision date
2016-09-29
Approval order statement
Location change for a component supplier.

Current openFDA PMA Record#

Device
UROVYSION BLADDER CANCER KIT
Applicant
Abbott Molecular
PMA number
P030052
Supplement
S018
Decision date
2016-09-29
Decision code
OK30
Date received
2016-09-02
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Location change for a component supplier.