Medical Device Manufacturer · US , Mchenry , IL

Inter-Med Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1984

Total

Cleared

Denied

Inter-Med Corp. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1984 to 1987. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Inter-Med Corp. Filter by specialty or product code using the sidebar.

Inter-Med Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Inter-Med Corp.

4 devices

1-4 of 4