Medical Device Manufacturer · US , Chicago , IL

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

5 submissions · 4 cleared · Since 1991

Total

Cleared

Denied

Prism Technologies, Inc. has 4 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 4 cleared submissions from 1991 to 1998. Primary specialty: Physical Medicine.

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

Prism 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 - Prism Technologies, Inc.

5 devices

1-5 of 5