VersaCross™ RF Wire
K-Number: K242076 · 2024-11-01
Device Summary
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. The listed applicant is Baylis Medical Company. The 510(k) number is K242076.
When did VersaCross™ RF Wire receive FDA 510(k) clearance?
VersaCross™ RF Wire received FDA 510(k) clearance on 2024-11-01, under 510(k) number K242076.
Who is the listed applicant for VersaCross™ RF Wire?
The FDA 510(k) record lists Baylis Medical Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VersaCross™ RF Wire?
The FDA product code for VersaCross™ RF Wire is DXF.
Other records listing Baylis Medical Company as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DXF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.