PMA P030005S061
- Device
- CONTAK RENEWAL TR FAMILY
- Applicant
- Guidant Corp.
- PMA number
- P030005
- Supplement
- S061
- Product code
- NKE
- Decision date
- 2010-03-04
- Classification
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (crt-p)
- Generic name
- Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
- Approval order statement
- ADDITION OF A REED SWITCH TEST AT THE REED SWITCH COMPONENT SUPPLIER.
Current openFDA PMA Record#
- Device
- CONTAK RENEWAL TR FAMILY
- Applicant
- Guidant Corp.
- PMA number
- P030005
- Supplement
- S061
- Product code
- NKE
- Generic name
- Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
- Decision date
- 2010-03-04
- Decision code
- OK30
- Date received
- 2010-02-04
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- ADDITION OF A REED SWITCH TEST AT THE REED SWITCH COMPONENT SUPPLIER.