Medical Device Manufacturer · US , Rosewell , GA

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

2 submissions · 2 cleared · Since 1995

Total

Cleared

Denied

Metrosoft, Inc. has 2 FDA 510(k) cleared medical devices. Based in Rosewell, US.

Historical record: 2 cleared submissions from 1995 to 1998. Primary specialty: Ophthalmic.

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

Metrosoft, 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 - Metrosoft, Inc.

2 devices

1-2 of 2