Medical Device Manufacturer · US , Washington , DC

Biomecca Australia , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1986

Total

Cleared

Denied

Biomecca Australia , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 1986 to 1986. Primary specialty: Cardiovascular.

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

Biomecca Australia , 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 - Biomecca Australia , Ltd.

2 devices

1-2 of 2