Medical Device Manufacturer · US , Fort Myers , FL

Kedl Internation Limited - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2008
1
Total
1
Cleared
0
Denied

Kedl Internation Limited has 1 FDA 510(k) cleared medical devices. Based in Fort Myers, US.

Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Kedl Internation Limited Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kedl Internation Limited
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