| Action Summary | The purpose of this action is to amend section 12VAC30-150-165 of the Durable Medical Equipment & Supplies (DME) regulations in order to align the regulations with federal requirements. |
| Chapters Affected | Only affects this chapter. |
| Executive Branch Review | This action will go through the normal Executive Branch Review process. |
| RIS Project | Yes [6938] |
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Is Federal action a driving factor in this regulatory change? If so, please provide a specific reference to the law, regulation
or court case.
2021 Appropriations Act (Special Session 1), Item QQQQQ
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| New Periodic Review | This action will not be used to conduct a new periodic review. |
| Name / Title: | Emily McClellan / Regulatory Supervisor |
| Address: |
Policy Division, DMAS 600 E. Broad Street, Suite 1300 Richmond, VA 23219 |
| Email Address: | Emily.McClellan@DMAS.Virginia.gov |
| Phone: | (804)371-4300 FAX: (804)786-1680 TDD: ()- |