Tomy International is one of 18904 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tomy International - FDA 510(k) Cleared Devices
Recent clearances: MEMORY PUMP MODEL Y4947
1
Total
1
Cleared
0
Denied
Tomy International has 1 FDA 510(k) cleared medical devices. Based in Canton, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Tomy International Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Tomy International
1 devices