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# Class 2 for Endoscopic Pancreatic Debridement Devices
- URL: https://www.fdaweb.com/class-2-for-endoscopic-pancreatic-debridement-devices/
- Published: 2024-09-09T12:00:00.000Z
- Updated: 2026-09-14T14:40:41.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5157732

*Federal Register* notice: FDA is classifying endoscopic pancreatic debridement devices into Class 2 (special controls). The action is based on a de novo classification request submitted by Interscope, Inc. for its EndoRotor device. The device is designed to endoscopically remove necrotic tissue from a walled-off pancreatic necrosis cavity. The device is inserted via an endoscope through a cystogastrostomy fistula into the pancreatic cavity. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2024-09-09/pdf/2024-20248.pdf?ref=fdaweb.com).