Medical Device Manufacturer · US , West Chester , OH

Corisen Group, Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Total

Cleared

Denied

Corisen Group, Ltd. has 1 FDA 510(k) cleared medical devices. Based in West Chester, US.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Obstetrics & Gynecology.

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

1 devices

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