Kamiya Biomedical Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kamiya Biomedical Co. - FDA 510(k) Cleared Devices
43
Total
43
Cleared
0
Denied
Kamiya Biomedical Co. has 43 FDA 510(k) cleared medical devices. Based in Thousand Oaks, US.
Historical record: 43 cleared submissions from 1991 to 2010. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Kamiya Biomedical Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kamiya Biomedical Co.
43 devices
Cleared
Sep 28, 2010
K-ASSAY CYSTATIN C REAGENT, CALIBRATOR AND CONTROL
Chemistry
358d
Cleared
Apr 29, 2010
K-ASSAY MICROALBUMIN AND K-ASSAY MICROALBUMIN CALIBRATOR
Chemistry
345d
Cleared
Dec 23, 2005
K-ASSAY FERRITIN (2) & FERRITIN CALIBRATOR SET
Immunology
253d
Cleared
Dec 10, 2004
K-ASSAY TOTAL IGE, K-ASSAY IGE CALIBRATOR SET, MODELS KAI-092/KAI-093C
Immunology
113d
Cleared
Jun 27, 2003
K-ASSAY D-DIMER, K-ASSAY D-DIMER CALIBRATOR, MODELS KAI-090
Hematology
114d
Cleared
Feb 04, 2003
K-ASSAY C-REACTIVE PROTEIN (3), K-ASSAY CRP MULTI-CALIBRATOR D, K-ASSAY CRP...
Immunology
78d
Cleared
Dec 13, 2002
K-ASSAY LP(A) CONTROLS
Immunology
24d
Cleared
Aug 14, 2002
K-ASSAY HS-CRP CONTROLS
Immunology
16d
Cleared
Jul 25, 2002
K-ASSAY LP(A) ASSAY
Chemistry
66d
Cleared
Feb 19, 2002
K-ASSAY FERRITIN, K-ASSAY FERRITIN CALIBRATOR SET
Immunology
53d
Cleared
Aug 21, 2001
K-ASSAY D-DIMER CONTROLS
Hematology
22d
Cleared
Jul 25, 2001
K-ASSAY C1-INA
Immunology
48d
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