Decision Date2026-01-18
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Baylis Connector Cable is the device name listed in this FDA 510(k) record. The listed applicant is Baylis Medical Technologies, Inc.. It received FDA 510(k) clearance on 2026-01-18 under 510(k) 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. The listed applicant is Baylis Medical Technologies, Inc.. The 510(k) number is K254114.
When did Baylis Connector Cable receive FDA 510(k) clearance?
Baylis Connector Cable received FDA 510(k) clearance on 2026-01-18, under 510(k) number K254114.
Who is the listed applicant for Baylis Connector Cable?
The FDA 510(k) record lists Baylis Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Baylis Connector Cable?
The FDA product code for Baylis Connector Cable is DSA.
Other records listing Baylis Medical Technologies, Inc. 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: DSA)
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.
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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.