Alere Scarborough, Inc D/B/A Binax, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alere Scarborough, Inc D/B/A Binax, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
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.
Alere Scarborough, Inc D/B/A Binax, Inc. — FDA 510(k) Products and Clearance History
4 devices
Cleared
Jun 13, 2014
ALERE I INFLUENZA A & B
Microbiology
4d
Cleared
Dec 18, 2013
ALERE INFLUENZA A & B TEST
Microbiology
41d
Cleared
Dec 05, 2013
ALERE BINAXNOW INFLUENZA A & B CARD
Microbiology
28d
Cleared
Jan 06, 2011
CLEARVIEW EXACT II INFLUENZA A & B TEST
Microbiology
28d