(1) An interested party may request the medicaid agency to include new medical equipment in the agency's medical equipment billing guide.
(2) The request must include credible evidence, including but not limited to:
(a) Manufacturer's literature;
(b) Manufacturer's pricing;
(c) Clinical research/case studies (including FDA approval, if required);
(d) Proof of certification from the Centers for Medicare and Medicaid Services (CMS), if applicable; and
(e) Any additional information the requester feels would aid the agency in its determination.
[Statutory Authority: RCW
41.05.021,
41.05.160 and 42 C.F.R. Part 440.70; 42 U.S.C. section 1396 (b)(i)(27). WSR 18-24-021, § 182-543-2100, filed 11/27/18, effective 1/1/19. Statutory Authority: RCW
41.05.021 and 2013 c 178. WSR 14-08-035, § 182-543-2100, filed 3/25/14, effective 4/25/14. WSR 11-14-075, recodified as § 182-543-2100, filed 6/30/11, effective 7/1/11. Statutory Authority: RCW
74.08.090 and
74.04.050. WSR 11-14-052, § 388-543-2100, filed 6/29/11, effective 8/1/11. Statutory Authority: RCW
74.04.050,
74.04.057,
74.08.090, and Public Law 104-191. WSR 03-19-083, § 388-543-2100, filed 9/12/03, effective 10/13/03. Statutory Authority: RCW
74.08.090,
74.09.530. WSR 01-01-078, § 388-543-2100, filed 12/13/00, effective 1/13/01.]