
[Federal Register Volume 80, Number 160 (Wednesday, August 19, 2015)]
[Notices]
[Pages 50292-50293]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-20397]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2015-N-2781]


Obstetrics and Gynecology Device Panel of the Medical Device 
Advisory Committee; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice; correction.

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SUMMARY: The Food and Drug Administration (FDA) is correcting a notice 
that appeared in the Federal Register of June 9, 2014 (79 FR 32964). 
Due to some recent confusion with the 2014 docket, this 2014 notice and 
all materials associated with it are being moved to a new docket. This 
document announces the new docket number.

FOR FURTHER INFORMATION CONTACT: Lisa Granger, Office of Policy, 
Planning,

[[Page 50293]]

Legislation, and Analysis, Food and Drug Administration, 10903 New 
Hampshire Ave., Bldg. 32, Rm. 3330, Silver Spring, MD 20993-0002, 301-
796-9115.

SUPPLEMENTARY INFORMATION: In FR Doc. 2014-13290, appearing on page 
32964, in the Federal Register of Monday, June 9, 2014, the following 
correction is made:
    On page 32964, in the second column, in the headings section of the 
document, [Docket No. FDA-2014-N-0736]'' is corrected to read ``FDA-
2015-N-2781''.
    Please be aware that this new docket is no longer open for comment.

    Dated: August 12, 2015.
Jill Hartzler Warner,
Associate Commissioner for Special Medical Programs.
[FR Doc. 2015-20397 Filed 8-18-15; 8:45 am]
 BILLING CODE 4164-01-P


