Focus Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Focus Technologies, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Focus Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in Cypress, US.
Historical record: 5 cleared submissions from 2002 to 2004. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Focus Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Focus Technologies, Inc.
5 devices
Cleared
Jun 30, 2004
WEST NILE VIRUS IGM CAPTURE ELISA
Microbiology
90d
Cleared
Oct 22, 2003
WEST NILE VIRUS IGM CAPTURE ELISA, MODEL EL0300M
Microbiology
119d
Cleared
Oct 22, 2003
WEST NILE VIRUS ELISA IGG, MODEL EL0300G
Microbiology
119d
Cleared
Aug 01, 2002
HERPESELECT 2 ELISA IGG, MODEL ELO920G
Microbiology
90d
Cleared
Jul 29, 2002
HERPESELECT 1 ELISA IGG, MODEL EL0910G
Microbiology
87d