Medical Device Manufacturer · US , Solana Beach , CA

Cross Vascular, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023
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
1-2 of 2
Cleared Oct 12, 2023
Cross Vascular RF Generator and Footswitch (optional accessory)
K232809 · GEI
General & Plastic Surgery · 30d
Cleared Oct 12, 2023
Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable
K232852 · DXF
Cardiovascular · 28d
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All2 General & Plastic Surgery 1 Cardiovascular 1