PMA P010012S239
- Device
- COGNIS/LIVIAN/RENEWAL 3 FAMILIES
- Applicant
- Boston Scientific Corp
- PMA number
- P010012
- Supplement
- S239
- Product code
- LWP
- Decision date
- 2010-04-15
- Classification
- Implantable Pulse Generator, Pacemaker (non-crt)
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Approval order statement
- CHANGES TO THE HYBRID CLEANING PROCESS TO ALIGN WITH OTHER PRODUCT LINES.
Current openFDA PMA Record#
- Device
- COGNIS/LIVIAN/RENEWAL 3 FAMILIES
- Applicant
- Boston Scientific Corp
- PMA number
- P010012
- Supplement
- S239
- Product code
- LWP
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Decision date
- 2010-04-15
- Decision code
- OK30
- Date received
- 2010-03-17
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGES TO THE HYBRID CLEANING PROCESS TO ALIGN WITH OTHER PRODUCT LINES.