[Federal Register Volume 84, Number 97 (Monday, May 20, 2019)] [Rules and Regulations] [Page 22702] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 2019-10399] [[Page 22702]] ======================================================================= ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 886 [Docket No. FDA-2018-N-3066] Medical Devices; Classification of Accessories Distinct From Other Devices; Finalized List of Accessories Suitable for Class I; Correction AGENCY: Food and Drug Administration, HHS. ACTION: Final classification action; correction. ----------------------------------------------------------------------- SUMMARY: The Food and Drug Administration (FDA) is correcting a document that appeared in the Federal Register of April 12, 2019. That document was published with the instruction to add a section to the incorrect subpart. This correction is being made to improve the accuracy of the final classification action. DATES: Effective May 20, 2019, and applicable May 13, 2019. FOR FURTHER INFORMATION CONTACT: Lisa Granger, Office of Policy and Planning, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 32, Rm. 3330, Silver Spring, MD 20993, 301-796-9115. SUPPLEMENTARY INFORMATION: In FR Doc. 2019-07290 appearing on page 14865 in the Federal Register of Friday, April 12, 2019, the following correction is made: Sec. 886.4355 [Corrected] 0 1. On page 14870, in the second column, in part 886, amendatory instruction 11 is corrected to read as follows: ``11. ``Add Sec. 886.4355 to subpart E to read as follows:'' Dated: May 14, 2019. Lowell J. Schiller, Principal Associate Commissioner for Policy. [FR Doc. 2019-10399 Filed 5-17-19; 8:45 am] BILLING CODE 4164-01-P