1
Total
1
Cleared
0
Denied
Mitsar Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in St. Petersburg, RU.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Mitsar Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nova Tech Eeg as regulatory consultant.
FDA 510(k) Regulatory Record - Mitsar Co., Ltd.
1 devices