PMA P160022S046

Device
X Series®; Propaq MD®; AED 3™ BLS; Zenix Professional Defibrillators
Applicant
ZOLL Medical Corporation
PMA number
P160022
Supplement
S046
Product code
MKJ
Decision date
2025-12-18
Classification
Cardiovascular
Generic name
Automated external defibrillators (non-wearable)
Approval order statement
approval for updates to the labeling to add post-approval study results.

Current openFDA PMA Record#

Device
X Series®; Propaq MD®; AED 3™ BLS; Zenix Professional Defibrillators
Applicant
ZOLL Medical Corporation
PMA number
P160022
Supplement
S046
Product code
MKJ
Generic name
Automated external defibrillators (non-wearable)
Decision date
2025-12-18
Decision code
APPR
Date received
2025-07-03
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - PAS
Approval order statement
approval for updates to the labeling to add post-approval study results.