Apnomed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Apnomed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ApnoDent Appliance
1
Total
1
Cleared
0
Denied
Apnomed, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bellevue, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Apnomed, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Dr. Colette Cozean, PHD as regulatory consultant.
FDA 510(k) Regulatory Record - Apnomed, Inc.
1 devices