Medical Device Manufacturer · US , Itasca , IL

Paraproducts, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

Total

Cleared

Denied

Paraproducts, Inc. has 1 FDA 510(k) cleared medical devices. Based in Itasca, US.

Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Paraproducts, Inc.

1 devices

1-1 of 1