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FDA 510(k)

Baylis Connector Cable

K-Number: K254114 · 2026-01-18

ApplicantBaylis Medical Technologies, Inc.
Decision Date2026-01-18
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Baylis Connector Cable is a medical device manufactured by Baylis Medical Technologies, Inc.. It received FDA 510(k) clearance on 2026-01-18 under approval number K254114. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Baylis Connector Cable?

Baylis Connector Cable is a medical device that received FDA 510(k) clearance on 2026-01-18. It is manufactured by Baylis Medical Technologies, Inc.. The 510(k) number is K254114.

When was Baylis Connector Cable approved by the FDA?

Baylis Connector Cable received FDA 510(k) clearance on 2026-01-18, under approval number K254114.

What company makes Baylis Connector Cable?

Baylis Connector Cable is manufactured by Baylis Medical Technologies, Inc..

What is the FDA product code for Baylis Connector Cable?

The FDA product code for Baylis Connector Cable is DSA.

Other Devices by Baylis Medical Technologies, Inc.

K230571RFP-100A Connector Cable (Single Use) K232562PowerWire Radiofrequency Guidewire Kit K250275PrecisePath™ Radiofrequency Puncture Generator and PrecisePath™ Footswitch K251158PowerWire® 14 Radiofrequency Guidewire Kit

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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.

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