Medical Device Manufacturer · US , Mchenry , IL

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

16 submissions · 15 cleared · Since 1976
16
Total
15
Cleared
0
Denied

Intermed, Inc. has 15 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 15 cleared submissions from 1976 to 1990. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Intermed, Inc.

16 devices
1-12 of 16
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