Apnicure, Inc. is one of 19157 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Apnicure, Inc. - FDA 510(k) Cleared Devices
Recent clearances: WINX SLEEP THERAPY SYSTEM, WINX SLEEP THERAPY SYSTEM, WINX SLEEP THERAPY SYSTEM
4
Total
4
Cleared
0
Denied
Apnicure, Inc. has 4 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 4 cleared submissions from 2012 to 2014. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Apnicure, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Apnicure, Inc.
4 devices