Tosoh Medics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tosoh Medics, Inc. - FDA 510(k) Cleared Devices
41
Total
41
Cleared
0
Denied
Tosoh Medics, Inc. has 41 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 41 cleared submissions from 1990 to 2002. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Tosoh Medics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tosoh Medics, Inc.
41 devices
Cleared
Dec 18, 2002
ST AIA-PACK CEA ENZYME IMMUNOASSAY
Immunology
26d
Cleared
Dec 17, 2002
ST AIA-PACK TESTOSTERONE ASSAY
Chemistry
91d
Cleared
Dec 17, 2002
ST AIA-PACK AFP ENZYME IMMUNOASSAY
Immunology
25d
Cleared
Dec 06, 2002
ST AIA-PACK CA 125 ENZYME IMMUNOASSAY
Immunology
14d
Cleared
May 14, 2002
G7 AUTOMATED HPLC ANALYZER, BETA-THALASSEMIA MODE
Hematology
90d
Cleared
Dec 14, 2001
AIA-PACK CTNI 2ND-GEN ASSAY
Chemistry
113d
Cleared
Sep 18, 2001
G7 AUTOMATED HPLC ANALYZER
Hematology
131d
Cleared
Aug 16, 2001
AIA-PACK BRCA, ST AIA PACK BRCA
Immunology
153d
Cleared
Aug 10, 1999
AIA-PACK FOLATE ASSAY
Chemistry
26d
Cleared
Jun 03, 1999
AIA-PACK CA 125
Immunology
112d
Cleared
May 11, 1999
AIA-PACK FT3 ASSAY
Chemistry
28d
Cleared
Dec 23, 1998
AIA-PACK TROPONIN I ASSAY
Chemistry
16d
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