Medical Device Manufacturer · US , Washington D.C. , DC

Evenflo Co., Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1996

Total

Cleared

Denied

Evenflo Co., Inc. has 3 FDA 510(k) cleared medical devices. Based in Washington D.C., US.

Historical record: 3 cleared submissions from 1996 to 1999. Primary specialty: Obstetrics & Gynecology.

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

Evenflo Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Evenflo Co., Inc.

3 devices

1-3 of 3