Medical Device Manufacturer · IL , Ginot Shomron 44853

A.Stein - Regulatory Affairs Consulting - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1997

Total

Cleared

Denied

A.Stein - Regulatory Affairs Consulting has 5 FDA 510(k) cleared medical devices. Based in Ginot Shomron 44853, IL.

Historical record: 5 cleared submissions from 1997 to 1999.

Browse the FDA 510(k) cleared devices submitted by A.Stein - Regulatory Affairs Consulting Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - A.Stein - Regulatory Affairs Consulting

5 devices

1-5 of 5