Medical Device Manufacturer · US , Minneapolis , MN

Menicon Co., Ltd. New Business Division - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2014
1
Total
1
Cleared
0
Denied

Menicon Co., Ltd. New Business Division has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Menicon Co., Ltd. New Business Division Filter by specialty or product code using the sidebar.

Menicon Co., Ltd. New Business Division — FDA 510(k) Products and Clearance History

1 devices
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