Medical Device Manufacturer · US , Waltham , MA

Rudolph Beaver, Inc. - FDA 510(k) Cleared Devices

6 submissions · 5 cleared · Since 1985

Total

Cleared

Denied

Rudolph Beaver, Inc. has 5 FDA 510(k) cleared medical devices. Based in Waltham, US.

Historical record: 5 cleared submissions from 1985 to 1988. Primary specialty: Ophthalmic.

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

FDA 510(k) Regulatory Record - Rudolph Beaver, Inc.

6 devices

1-6 of 6