[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]]

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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.

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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


