PMA P010012S067
- Device
- CONTAK RENEWAL/CD 2/RENEWAL RF FAMILIES
- Applicant
- Boston Scientific Corp
- PMA number
- P010012
- Supplement
- S067
- Product code
- LWP
- Decision date
- 2005-09-13
- Classification
- Implantable Pulse Generator, Pacemaker (non-crt)
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Approval order statement
- ADDITION OF AN INLINE TEMPERATURE AND HUMIDITY CONTROLLED CURE TUNNEL TO FILL CHANNELS.
Current openFDA PMA Record#
- Device
- CONTAK RENEWAL/CD 2/RENEWAL RF FAMILIES
- Applicant
- Boston Scientific Corp
- PMA number
- P010012
- Supplement
- S067
- Product code
- LWP
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Decision date
- 2005-09-13
- Decision code
- OK30
- Date received
- 2005-08-15
- Supplement type
- 30-Day Notice
- Approval order statement
- ADDITION OF AN INLINE TEMPERATURE AND HUMIDITY CONTROLLED CURE TUNNEL TO FILL CHANNELS.