Medical Device Manufacturer · US , Mchenry , IL

Cederroth, Inc. USA - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 1982

Total

Cleared

Denied

Cederroth, Inc. USA has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 6 cleared submissions from 1982 to 1988. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Cederroth, Inc. USA

7 devices

1-7 of 7