Medical Device Manufacturer · US , Mchenry , IL

Mec/Surgitek Products - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1983

Total

Cleared

Denied

Mec/Surgitek Products has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1983 to 1983. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Mec/Surgitek Products Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Mec/Surgitek Products

2 devices

1-2 of 2