PMA P010030S137
- Device
- LifeVest Wearable Defibrillator
- Applicant
- Zoll Manufacturing Corporation
- PMA number
- P010030
- Supplement
- S137
- Product code
- MVK
- Decision date
- 2020-05-14
- Generic name
- Wearable automated external defibrillator
- Approval order statement
- Change of the manufacturing test criteria for the gas generator in the LifeVest Model 4000 Therapy Electrodes.
Current openFDA PMA Record#
- Device
- LifeVest Wearable Defibrillator
- Applicant
- Zoll Manufacturing Corporation
- PMA number
- P010030
- Supplement
- S137
- Product code
- MVK
- Generic name
- Wearable automated external defibrillator
- Decision date
- 2020-05-14
- Decision code
- OK30
- Date received
- 2020-05-04
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Change of the manufacturing test criteria for the gas generator in the LifeVest Model 4000 Therapy Electrodes.