Ivd Research, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ivd Research, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Ivd Research, Inc. has 5 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Historical record: 5 cleared submissions from 2002 to 2009. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Ivd Research, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ivd Research, Inc.
5 devices
Cleared
Jan 14, 2009
GIARDIA FECAL ANTIGEN DETECTION LATERAL FLOW KIT, MODEL GL-LF
Microbiology
275d
Cleared
May 27, 2004
C. DIFFICILE TOXIN A + B FECAL ANTIGEN DETECTION MICROWELL ELISA KIT MODEL
Microbiology
253d
Cleared
Jul 10, 2003
IVD CRYPTOSPORIDIUM ANTIGEN DETECTION ASSAY, MODEL CP-96
Microbiology
104d
Cleared
Mar 05, 2003
IVD CRYPTO/GIARDIA DFA
Microbiology
82d
Cleared
Sep 17, 2002
IVD GIARDIA ANTIGEN DETECTION ASSAY MODEL GL-96
Microbiology
208d