Cross Vascular RF Generator and Footswitch (optional accessory)
K-Number: K232809 · 2023-10-12
Device Summary
Frequently Asked Questions
What is the Cross Vascular RF Generator and Footswitch (optional accessory)?
Cross Vascular RF Generator and Footswitch (optional accessory) is a medical device that received FDA 510(k) clearance on 2023-10-12. It is manufactured by Cross Vascular, Inc.. The 510(k) number is K232809.
When was Cross Vascular RF Generator and Footswitch (optional accessory) approved by the FDA?
Cross Vascular RF Generator and Footswitch (optional accessory) received FDA 510(k) clearance on 2023-10-12, under approval number K232809.
What company makes Cross Vascular RF Generator and Footswitch (optional accessory)?
Cross Vascular RF Generator and Footswitch (optional accessory) is manufactured by Cross Vascular, Inc..
What is the FDA product code for Cross Vascular RF Generator and Footswitch (optional accessory)?
The FDA product code for Cross Vascular RF Generator and Footswitch (optional accessory) is GEI.
Related Clinical Trials
Other Devices by Cross Vascular, Inc.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.