PMA P980016S112
- Device
- VARIOUS FAMILIES OF ICDS
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- PMA number
- P980016
- Supplement
- S112
- Product code
- LWS
- Decision date
- 2007-11-16
- Classification
- Implantable Cardioverter Defibrillator (non-crt)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Approval order statement
- ADDITION OF A PAPERLESS CHART RECORDER TO THE STERILIZATION OPERATIONS AT THE TOLOCHENAZ, SWITZERLAND MANUFACTURING FACILITY.
Current openFDA PMA Record#
- Device
- VARIOUS FAMILIES OF ICDS
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- PMA number
- P980016
- Supplement
- S112
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 2007-11-16
- Decision code
- OK30
- Date received
- 2007-10-11
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- ADDITION OF A PAPERLESS CHART RECORDER TO THE STERILIZATION OPERATIONS AT THE TOLOCHENAZ, SWITZERLAND MANUFACTURING FACILITY.