Medical Device Manufacturer · US , Anaheim , CA

Sechrist - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1991

Total

Cleared

Denied

Sechrist has 2 FDA 510(k) cleared medical devices. Based in Anaheim, US.

Historical record: 2 cleared submissions from 1991 to 1993. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Sechrist

2 devices

1-2 of 2