PMA P110042S013
- Device
- SUBCUTANEOUS IMPLANTABLE DEFIBRILLATOR (S-ICD) SYSTEM
- Applicant
- Boston Scientific Corporation
- PMA number
- P110042
- Supplement
- S013
- Product code
- LWS
- Decision date
- 2013-08-22
- Classification
- Implantable Cardioverter Defibrillator (non-crt)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Approval order statement
- PERFORM RECEIVING AND INSPECTION ACTIVITIES FOR CERTAIN COMPONENTS AND ACCESSORIES USED IN THE CAMERON HEALTH, INC. S-ICD SYSTEM AT BOSTON SCIENTIFIC CORPORATIONS MANUFACTURING FACILITY LOCATED IN ST PAUL, MINNESOTA.
Current openFDA PMA Record#
- Device
- SUBCUTANEOUS IMPLANTABLE DEFIBRILLATOR (S-ICD) SYSTEM
- Applicant
- Boston Scientific Corporation
- PMA number
- P110042
- Supplement
- S013
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 2013-08-22
- Decision code
- OK30
- Date received
- 2013-08-01
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- PERFORM RECEIVING AND INSPECTION ACTIVITIES FOR CERTAIN COMPONENTS AND ACCESSORIES USED IN THE CAMERON HEALTH, INC. S-ICD SYSTEM AT BOSTON SCIENTIFIC CORPORATIONS MANUFACTURING FACILITY LOCATED IN ST PAUL, MINNESOTA.