PMA P160032S007

Device
Lifeline/ReviveR, Lifeline/ReviveR Auto, Lifeline/ReviveR VIEW, Lifeline/ReviveR VIEW AUTO, Lifeline/ReviveR ECG, and Li
Applicant
Defibtech, LLC
PMA number
P160032
Supplement
S007
Product code
MKJ
Decision date
2020-06-23
Generic name
Automated external defibrillators (non-wearable)
Approval order statement
Implementation of a replacement furnace that is used in the manufacture of a diode component used in the device circuit boards.

Current openFDA PMA Record#

Device
Lifeline/ReviveR, Lifeline/ReviveR Auto, Lifeline/ReviveR VIEW, Lifeline/ReviveR VIEW AUTO, Lifeline/ReviveR ECG, and Li
Applicant
Defibtech, LLC
PMA number
P160032
Supplement
S007
Product code
MKJ
Generic name
Automated external defibrillators (non-wearable)
Decision date
2020-06-23
Decision code
OK30
Date received
2020-05-26
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Implementation of a replacement furnace that is used in the manufacture of a diode component used in the device circuit boards.