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# Info Collection Extension for Device Reclassification Petitions
- URL: https://www.fdaweb.com/info-collection-extension-for-device-reclassification-petitions/
- Published: 2018-08-07T12:00:00.000Z
- Updated: 2026-09-15T00:24:10.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5142055

*Federal Register* notice: FDA has submitted to OMB an information collection extension for “Reclassification Petitions for Medical Devices” (OMB Control Number 0910-0138). Agency regulations give it the responsibility to collect data and information contained in such petitions, which allow any person to petition for reclassification of a device from any of the three classes (Class 1, 2 or 3). To view the notice, click [here](https://s3.amazonaws.com/public-inspection.federalregister.gov/2018-16983.pdf?ref=fdaweb.com).