PMA P910073S150
- Device
- Endotak Reliance, Reliance 4-Front
- Applicant
- Boston Scientific
- PMA number
- P910073
- Supplement
- S150
- Product code
- LWS
- Decision date
- 2018-07-26
- Classification
- Implantable Cardioverter Defibrillator (non-crt)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Approval order statement
- Implement the Central Monitoring System for the monitoring of environmental conditions at the Dorado facility.
Current openFDA PMA Record#
- Device
- Endotak Reliance, Reliance 4-Front
- Applicant
- Boston Scientific
- PMA number
- P910073
- Supplement
- S150
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 2018-07-26
- Decision code
- OK30
- Date received
- 2018-07-13
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Implement the Central Monitoring System for the monitoring of environmental conditions at the Dorado facility.