Keyamed Na, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Keyamed Na, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DEEPVESSEL FFR
1
Total
1
Cleared
0
Denied
Keyamed Na, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seattle, US.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Keyamed Na, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Keyamed Na, Inc.
1 devices