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FDA 510(k)

Cross Vascular RF Generator and Footswitch (optional accessory)

K-Number: K232809 · 2023-10-12

Decision Date2023-10-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Cross Vascular RF Generator and Footswitch (optional accessory) is a medical device manufactured by Cross Vascular, Inc.. It received FDA 510(k) clearance on 2023-10-12 under approval number K232809. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

Related Devices (Code: GEI)

Official Source

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