Medical Device Manufacturer · US , Largo , FL

Burke Neutech, Inc. - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 1993

Total

Cleared

Denied

Burke Neutech, Inc. has 6 FDA 510(k) cleared medical devices. Based in Largo, US.

Historical record: 6 cleared submissions from 1993 to 1996. Primary specialty: Physical Medicine.

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

Burke Neutech, 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 - Burke Neutech, Inc.

7 devices

1-7 of 7