Medical Device Manufacturer · US , Washington , DC

Ime Co. , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987
2
Total
2
Cleared
0
Denied

Ime Co. , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 1987 to 1988. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Ime Co. , Ltd.

2 devices
1-2 of 2
Filters