Medical Device Manufacturer · US , Mchenry , IL

Diagnon Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1983

Total

Cleared

Denied

Diagnon Corp. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 6 cleared submissions from 1983 to 1986. Primary specialty: Microbiology.

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

Diagnon 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 - Diagnon Corp.

6 devices

1-6 of 6