Medical Device Manufacturer · US , Kansas City , MO

Southwest Technologies, Inc. - FDA 510(k) Cleared Devices

5 submissions · 3 cleared · Since 1987

Total

Cleared

Denied

Southwest Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Kansas City, US.

Historical record: 3 cleared submissions from 1987 to 2010. Primary specialty: General & Plastic Surgery.

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

Southwest Technologies, 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 - Southwest Technologies, Inc.

5 devices

1-5 of 5