Aearo Co. is one of 25408 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aearo Co. - FDA 510(k) Cleared Devices
Recent clearances: PLEATS PLUS N95 PARTICULATE RESPIRATOR, MODELS 1050 AND 1050S
1
Total
1
Cleared
0
Denied
Aearo Co. has 1 FDA 510(k) cleared medical devices. Based in Southbridge, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Aearo Co. 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 - Aearo Co.
1 devices