Ivd Research, Inc. is one of 26109 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
Recent clearances: GIARDIA FECAL ANTIGEN DETECTION LATERAL FLOW KIT, MODEL GL-LF, C. DIFFICILE TOXIN A + B FECAL ANTIGEN DETECTION MICROWELL ELISA KIT MODEL, IVD CRYPTOSPORIDIUM ANTIGEN DETECTION ASSAY, MODEL CP-96
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.
510(k) submissions have been managed by California Department of Health Services as regulatory consultant.
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