PMA P110042S082
- Device
- All Flex 4-Socket Hi-POT/Pulse Test System
- Applicant
- Boston Scientific Corporation
- PMA number
- P110042
- Supplement
- S082
- Product code
- LWS
- Decision date
- 2017-04-23
- Classification
- Implantable Cardioverter Defibrillator (non-crt)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Approval order statement
- Addition of automated test equipment to perform leakage current and resistance acceptance activities.
Current openFDA PMA Record#
- Device
- All Flex 4-Socket Hi-POT/Pulse Test System
- Applicant
- Boston Scientific Corporation
- PMA number
- P110042
- Supplement
- S082
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 2017-04-23
- Decision code
- OK30
- Date received
- 2017-03-29
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Addition of automated test equipment to perform leakage current and resistance acceptance activities.