|Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.|
|Trade Name||DISCOVERY, MERIDIAN|
|Classification Name||implantable pulse generator, pacemaker (non-crt)|
|Generic Name||dual-chamber adaptive-rate pacemaker|
|Supplement Type||30-day notice|
|Expedited Review Granted?|| No|
|Approval Order Statement |
Changes in procedures for cytotoxicity and pyrogenicity testing for inspections of incoming components.