|Trade Name||DISCOVERY/ MERIDIAN|
|Classification Name||implantable pulse generator, pacemaker (non-crt)|
|Generic Name||dual-chamber adaptive-rate pacemaker|
|Supplement Type||normal 180 day track|
|Supplement Reason|| labeling change - instructions|
|Expedited Review Granted?|| No|
|Approval Order Statement |
Approval for product reliability test to be added to the physician and patient labeling as well as other minor changes to the patient manuals.