Intravu, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intravu, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MIDASVu, MIDAScope and Introducer Kit, and MIDASystem
2
Total
2
Cleared
0
Denied
Intravu, Inc. has 2 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Latest FDA clearance: Dec 2024. Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Intravu, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Intravu, Inc.
2 devices