PMA P090013S282
- Device
- Revo MRI
- Applicant
- Medtronic, Inc.
- PMA number
- P090013
- Supplement
- S282
- Product code
- LWP
- Decision date
- 2018-05-30
- Classification
- Implantable Pulse Generator, Pacemaker (non-crt)
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Approval order statement
- Approval for updates to the Medtronic MyCareLink Patient Monitor Models 24950 and 24952.
Current openFDA PMA Record#
- Device
- Revo MRI
- Applicant
- Medtronic, Inc.
- PMA number
- P090013
- Supplement
- S282
- Product code
- LWP
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Decision date
- 2018-05-30
- Decision code
- APPR
- Date received
- 2018-04-17
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- Approval for updates to the Medtronic MyCareLink Patient Monitor Models 24950 and 24952.