Cosmo Technologies, Ltd. is one of 87 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Cosmo Technologies, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SIC 8000
1
Total
1
Cleared
0
Denied
Cosmo Technologies, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Dublin 1, IE.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cosmo Technologies, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Conventus Biomedical Solutions, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cosmo Technologies, Ltd.
1 devices