Medical Device Manufacturer · US , Rochester , NY

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

4 submissions · 4 cleared · Since 2003

Total

Cleared

Denied

Getinge USA, Inc. has 4 FDA 510(k) cleared medical devices. Based in Rochester, US.

Historical record: 4 cleared submissions from 2003 to 2005. Primary specialty: General Hospital.

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

Getinge USA, 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 - Getinge USA, Inc.

4 devices

1-4 of 4