Binax, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Binax, Inc. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
Binax, Inc. has 30 FDA 510(k) cleared microbiology devices. Based in S. Portland, US.
Historical record: 30 cleared submissions from 1986 to 2010.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Binax, Inc.
30 devices
Cleared
Apr 14, 2010
BINAXNOW PBP2A TEST, MODEL 890-000
Microbiology
432d
Cleared
Feb 24, 2010
CLEARVIEW EXACT PBP2A TEST, MODEL 891-000
Microbiology
252d
Cleared
Dec 16, 2009
BINAXNOX STAPHYLOCOCCUS AUREUS TEST
Microbiology
254d
Cleared
Sep 04, 2009
CLEARVIEW ADVANCED STREP A , MODEL 737-430
Microbiology
107d
Cleared
Sep 01, 2009
BINAXNOW MALARIA POSITIVE CONTROL KIT, MODEL 665-010
Microbiology
259d
Cleared
Aug 12, 2009
MODIFICATION TO: BINAXNOW INFLUENZA A & B TEST
Microbiology
20d
Cleared
Oct 23, 2008
BINAXNOW G6PD TEST
Hematology
295d
Cleared
Nov 09, 2006
BINAXNOW INFLUENZA A & B TEST
Microbiology
108d
Cleared
Nov 30, 2005
BINAXNOW INFLUENZA A & B TEST
Microbiology
23d
Cleared
Aug 10, 2004
BINAXNOW INFLUENZA A & B TEST
Microbiology
110d
Cleared
Oct 21, 2003
BINAX NOW RSV TEST, MODEL 430-000 AND BINAX NOW NASOPHARYNGEAL SWAB ACCESSORY...
Microbiology
97d
Cleared
Sep 19, 2002
BINAX NOW FLU B TEST (27 TEST), BINAX NOW NASOPHARYNGEAL SWAB SPECIMEN...
Microbiology
122d