Fujimori Kogyo, Co., Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Fujimori Kogyo, Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: T-TAS 01 Total Thrombus-formation Analysis System Instrument, PL Chip for T-TAS 01, PL Chip Reservoir Set for T-TAS 01, BAPA tube for T-TAS 01
1
Total
1
Cleared
0
Denied
Fujimori Kogyo, Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Shinjuku, Tokyo, JP.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Fujimori Kogyo, Co., Ltd. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Fujimori Kogyo, Co., Ltd.
1 devices