Aearo Company is one of 24660 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aearo Company - FDA 510(k) Cleared Devices
Recent clearances: AEARO COMPANY SURGICAL N95 RESPIRATORS, MODELS N9508C AND N9511C, N95 RESPIRATOR, MODELS N9504C, N9504CS AND N9514C, PLEATS PLUS N95 RESPIRATOR, MODELS 1054 AND 1054S
3
Total
3
Cleared
0
Denied
Aearo Company has 3 FDA 510(k) cleared medical devices. Based in Southbridge, US.
Historical record: 3 cleared submissions from 2006 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Aearo Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aearo Company
3 devices