Medical Device Manufacturer · US , Mchenry , IL

Respitrace Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1978

Total

Cleared

Denied

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

Historical record: 6 cleared submissions from 1978 to 1986. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Respitrace Corp.

6 devices

1-6 of 6