Medical Device Manufacturer · US , Camp Hill , PA

Enteron, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1988

Total

Cleared

Denied

Enteron, Inc. has 1 FDA 510(k) cleared medical devices. Based in Camp Hill, US.

Historical record: 1 cleared submissions from 1988 to 1988. Primary specialty: Chemistry.

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

1 devices

1–1 of 1