Medical Device Manufacturer · US , Mundelein , IL

Maersk Medical, Ltd. - FDA 510(k) Cleared Devices

4 submissions · 2 cleared · Since 1997

Total

Cleared

Denied

Maersk Medical, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Mundelein, US.

Historical record: 2 cleared submissions from 1997 to 2001. Primary specialty: General & Plastic Surgery.

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

Maersk Medical, Ltd. 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 - Maersk Medical, Ltd.

4 devices

1-4 of 4