American Bio Medica Corp. is one of 5299 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Bio Medica Corp. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
American Bio Medica Corp. has 30 FDA 510(k) cleared toxicology devices. Based in Washington, US.
Historical record: 30 cleared submissions from 1997 to 2017.
Browse the complete list of FDA 510(k) cleared toxicology devices from this manufacturer. Filter by specialty or product code using the sidebar.
American Bio Medica Corp. — FDA 510(k) Products and Clearance History
30 devices
Cleared
Aug 15, 2017
Rapid Tox Cup II
Toxicology
202d
Cleared
May 30, 2008
RAPID TOX CUP
Toxicology
212d
Cleared
Aug 07, 2006
RAPIDONE-BUPRENORPHINE TEST
Toxicology
139d
Cleared
Jun 15, 2006
RAPIDONE-COCAINE-150 TEST
Toxicology
189d
Cleared
May 25, 2006
RAPIDTOX
Toxicology
174d
Cleared
Jul 12, 2005
RAPID READER
Chemistry
385d
Cleared
Nov 03, 2004
'RAPIDTEC 4' TEST
Toxicology
133d
Cleared
May 22, 2003
'RAPID ONE' - PROPOXYPHENE TEST
Toxicology
66d
Cleared
Apr 30, 2003
'RAPIDTEC'-5M-MULTIPLE DIP TEST
Toxicology
161d
Cleared
Jul 23, 2002
'RAPIDTEC' 5A MULTIPLE DIP TEST
Toxicology
109d
Cleared
Mar 20, 2002
RAPIDONE-OXY TEST
Toxicology
97d
Cleared
Nov 26, 2001
RAPIDONE-ECSTASY TEST
Toxicology
63d