PMA P030005S068
- Device
- H120 & H125 CONTAK RENEWAL TR IS-1
- Applicant
- Guidant Corp.
- PMA number
- P030005
- Supplement
- S068
- Product code
- NKE
- Decision date
- 2010-09-03
- Classification
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (crt-p)
- Generic name
- Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
- Approval order statement
- CHANGES TO TEST SOFTWARE USED TO PERFORM ELECTRICAL TESTING OF INTEGRATED CIRCUITS USED IN PULSE GENERATORS.
Current openFDA PMA Record#
- Device
- H120 & H125 CONTAK RENEWAL TR IS-1
- Applicant
- Guidant Corp.
- PMA number
- P030005
- Supplement
- S068
- Product code
- NKE
- Generic name
- Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
- Decision date
- 2010-09-03
- Decision code
- OK30
- Date received
- 2010-08-06
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGES TO TEST SOFTWARE USED TO PERFORM ELECTRICAL TESTING OF INTEGRATED CIRCUITS USED IN PULSE GENERATORS.