Medical Device Manufacturer · US , Madison , WI

Minitube of America, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Total

Cleared

Denied

Minitube of America, Inc. has 2 FDA 510(k) cleared medical devices. Based in Madison, US.

Historical record: 2 cleared submissions from 2006 to 2006. Primary specialty: Obstetrics & Gynecology.

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

Minitube of America, 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 - Minitube of America, Inc.

2 devices

1-2 of 2