Medical Device Manufacturer · JP , Shinjuku, Tokyo

Fujimori Kogyo, Co., Ltd.

1 submissions · 1 cleared · Since 2020
1
Total
1
Cleared
0
Denied

Fujimori Kogyo, Co., Ltd. — FDA 510(k) Submissions

Fujimori Kogyo, Co., Ltd. has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Automated Platelet Aggregation . Use the specialty filter in the sidebar to narrow results.

1 devices
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All1 Hematology 1