Medical Device Manufacturer · US , St. Petersburg , FL

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

3 submissions · 3 cleared · Since 1987

Total

Cleared

Denied

Human Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in St. Petersburg, US.

Historical record: 3 cleared submissions from 1987 to 1988. Primary specialty: General Hospital.

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

Human 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 - Human Technologies, Inc.

3 devices

1-3 of 3