Quidel Cardiovascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Quidel Cardiovascular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Quidel Triage® TOX Drug Screen, 94600, Quidel Triage TOX Drug Screen, 94600
2
Total
2
Cleared
0
Denied
Quidel Cardiovascular, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Deigo, US.
Historical record: 2 cleared submissions from 2019 to 2020. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Quidel Cardiovascular, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Quidel Cardiovascular, Inc.
2 devices