Medical Device Manufacturer · US , Scarborough , ME

Alere Scarborough, Inc D/B/A Binax, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2011

Total

Cleared

Denied

Alere Scarborough, Inc D/B/A Binax, Inc. has 4 FDA 510(k) cleared medical devices. Based in Scarborough, US.

Historical record: 4 cleared submissions from 2011 to 2014. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Alere Scarborough, Inc D/B/A Binax, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Alere Scarborough, Inc D/B/A Binax, Inc.

4 devices

1-4 of 4