Quidel Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Quidel Corp. - FDA 510(k) Cleared Devices
Recent clearances: QUIDEL MOLECULAR RSV + HMPV ASSAY, QUIDEL MOLECULAR INFLUENZA A + B ASSAY, SOFIA(R) RSV FIA
93
Total
93
Cleared
0
Denied
Quidel Corp. has 93 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 93 cleared submissions from 1983 to 2013. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Quidel Corp. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Quidel Corp.
93 devices
Cleared
Sep 06, 2013
QUIDEL MOLECULAR RSV + HMPV ASSAY
Microbiology
78d
Cleared
Aug 29, 2013
QUIDEL MOLECULAR INFLUENZA A + B ASSAY
Microbiology
78d
Cleared
CT
Aug 13, 2013
SOFIA(R) RSV FIA
Microbiology
175d
Cleared
Aug 02, 2013
SOFIA(R) HCG FIA
Chemistry
100d
Cleared
Jul 05, 2013
SOFIA INFLUENZA A+B FIA
Microbiology
32d
Cleared
Jun 28, 2013
QUICKVUE INFLUENZA A+B
Microbiology
25d
Cleared
Mar 08, 2013
QUIDEL MOLECULAR RSV + HMPV ASSAY
Microbiology
227d
Cleared
Mar 08, 2013
QUIDEL MOLECULAR DIRECT C. DIFFICILE ASSAY
Microbiology
72d
Cleared
Mar 15, 2012
QUIDEL MOLECULAR INFLUENZA A+B
Microbiology
85d
Cleared
Dec 22, 2011
QUIDEL MOLECULAR INFLUENZA A + B ASSAY
Microbiology
147d
Cleared
Dec 15, 2011
QUIDEL MOLECULAR HMPV ASSAY
Microbiology
108d
Cleared
Oct 24, 2011
SOFIA ANALYZER AND INFLUENZA A+B FIA
Microbiology
88d
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