Medical Device Manufacturer · US , Mchenry , IL

Mistogen Equipment Co. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1976

Total

Cleared

Denied

Mistogen Equipment Co. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1976 to 1980. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Mistogen Equipment Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Mistogen Equipment Co.

4 devices

1-4 of 4