Oconnell Regulatory Consultants, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oconnell Regulatory Consultants, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vivo 45 LS
1
Total
1
Cleared
0
Denied
Oconnell Regulatory Consultants, Inc. has 1 FDA 510(k) cleared medical devices. Based in Stoneham, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Oconnell Regulatory Consultants, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oconnell Regulatory Consultants, Inc.
1 devices