PMA P910073S152
- Device
- Reliance 4-Front Lead Family (passive fixation models)
- Applicant
- Boston Scientific
- PMA number
- P910073
- Supplement
- S152
- Product code
- LWS
- Decision date
- 2019-01-10
- Classification
- Implantable Cardioverter Defibrillator (non-crt)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Approval order statement
- Change the authorized laboratory for testing USP grade polyethylene glycol (PEG) 3350 and mannitol material to other service providers.
Current openFDA PMA Record#
- Device
- Reliance 4-Front Lead Family (passive fixation models)
- Applicant
- Boston Scientific
- PMA number
- P910073
- Supplement
- S152
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 2019-01-10
- Decision code
- OK30
- Date received
- 2018-12-20
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Change the authorized laboratory for testing USP grade polyethylene glycol (PEG) 3350 and mannitol material to other service providers.