Aerogen (Ireland), Ltd. is one of 89 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Aerogen (Ireland), Ltd. - FDA 510(k) Cleared Devices
Recent clearances: NIVO NEBULIZER SYSTEM, AERONEB GO NEBULIZER, AERONEB PROFESSIONAL NEBULIZER SYSTEM
3
Total
3
Cleared
0
Denied
Aerogen (Ireland), Ltd. has 3 FDA 510(k) cleared medical devices. Based in Dangan Galway, IE.
Historical record: 3 cleared submissions from 2007 to 2010. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Aerogen (Ireland), Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aerogen Ireland, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Aerogen (Ireland), Ltd.
3 devices