K254114
- 510(k) number
- K254114
- Device name
- Baylis Connector Cable
- Applicant
- Baylis Medical Technologies, Inc. CA
- Product code
- DSA — Cable, Transducer And Electrode, Patient, (Including
- Decision date
- 2026-01-18
- Date received
- 2025-12-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain
Also available from FDA: K254114.pdf
Official FDA record: K254114
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.