FDA vaccine official restricted COVID vaccine approvals against the advice of agency staff

FILE - The U.S. Food and Drug Administration campus in Silver Spring, Md., is photographed, Oct. 14, 2015. (AP Photo/Andrew Harnik, File)

WASHINGTON (AP) — U.S. regulators have approved the first cervical cancer testing kit that allows women to collect their own sample at home before shipping it to a laboratory, according to a medical device company.

Teal Health said Friday the Food and Drug Administration approved its Teal Wand for home use, offering a new way to collect vaginal samples that can detect the HPV virus that causes cervical cancer. Currently, HPV tests and Pap smears are performed at a health clinic or doctor's office.

The ɫtv Press. All rights reserved.

More Health Stories

Sign Up to Newsletters

Get the latest from ɫtvNews in your inbox. Select the emails you're interested in below.