Medical Device Manufacturer · US , Mchenry , IL

Keymed, Inc. - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 1981
29
Total
29
Cleared
0
Denied

Keymed, Inc. has 29 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 29 cleared submissions from 1981 to 2010. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Keymed, Inc.
29 devices
1-12 of 29
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