Ferrania USA, Inc. is one of 25828 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ferrania USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE
1
Total
1
Cleared
0
Denied
Ferrania USA, Inc. has 1 FDA 510(k) cleared medical devices. Based in Weatherford, US.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ferrania USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ferrania USA, Inc.
1 devices