Cross Vascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cross Vascular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cross Vascular RF Generator and Footswitch (optional accessory), Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable
2
Total
2
Cleared
0
Denied
Cross Vascular, Inc. has 2 FDA 510(k) cleared medical devices. Based in Solana Beach, US.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cross Vascular, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cross Vascular, Inc.
2 devices