Toyobo Co., Ltd. is one of 154 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Toyobo Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Kita-Ku, JP.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Toyobo Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Epstein Becker & Green, P.C. as regulatory consultant.
FDA 510(k) Regulatory Record - Toyobo Co., Ltd.
1 devices