Medical Device Manufacturer · US , Washington , DC

Ultrafem, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1993

Total

Cleared

Denied

Ultrafem, Inc. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 1993 to 1997. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Ultrafem, Inc. Filter by specialty or product code using the sidebar.

Ultrafem, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ultrafem, Inc.

2 devices

1-2 of 2