FDA 510(k)

VersaCross RF Wire

K-Number: K242076 · 2024-11-01

Decision Date2024-11-01

Product CodeDXF

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

VersaCross RF Wire is a medical device manufactured by Baylis Medical Company. It received FDA 510(k) clearance on 2024-11-01 under approval number K242076. The device is classified under product code DXF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VersaCross RF Wire?

VersaCross RF Wire is a medical device that received FDA 510(k) clearance on 2024-11-01. It is manufactured by Baylis Medical Company. The 510(k) number is K242076.

When was VersaCross RF Wire approved by the FDA?

VersaCross RF Wire received FDA 510(k) clearance on 2024-11-01, under approval number K242076.

What company makes VersaCross RF Wire?

VersaCross RF Wire is manufactured by Baylis Medical Company.

What is the FDA product code for VersaCross RF Wire?

The FDA product code for VersaCross RF Wire is DXF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.