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# EPPG Devices and Pacing System Analyzers into Class 2
- URL: https://www.fdaweb.com/eppg-devices-and-pacing-system-analyzers-into-class-2/
- Published: 2016-04-18T12:00:00.000Z
- Updated: 2026-09-14T20:55:28.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5135413

*Federal Register* Final order: FDA is issuing a final order to reclassify external pacemaker pulse generator (EPPG) devices, which are currently preamendments Class 3 devices (regulated under product code DTE), into Class 2 (special controls) and to reclassify pacing system analyzers (PSAs) into Class 2 based on new information and subject to premarket notification. This final order also creates a separate classification regulation for PSAs and places single and dual chamber PSAs, which are currently classified with EPPG devices, and triple chamber PSAs (TCPSAs), which are currently postamendments Class 3 devices, into that new classification regulation. To view this notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2016-04-18/pdf/2016-08898.pdf?ref=fdaweb.com).