PMA P160022S009
- Device
- X Series/Propaq MD
- Applicant
- ZOLL Medical Corporation
- PMA number
- P160022
- Supplement
- S009
- Product code
- MKJ
- Decision date
- 2019-03-21
- Classification
- Automated External Defibrillators (non-wearable)
- Generic name
- Automated external defibrillators (non-wearable)
- Approval order statement
- Automation of the power supply measurement test for the system board.
Current openFDA PMA Record#
- Device
- X Series/Propaq MD
- Applicant
- ZOLL Medical Corporation
- PMA number
- P160022
- Supplement
- S009
- Product code
- MKJ
- Generic name
- Automated external defibrillators (non-wearable)
- Decision date
- 2019-03-21
- Decision code
- OK30
- Date received
- 2019-03-19
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Automation of the power supply measurement test for the system board.