# K254114: Baylis Connector Cable

- Pathway: 510(k) (Special)
- Applicant: Baylis Medical Technologies, Inc.
- Decided: Jan 18, 2026 after 30 days
- Product code: DSA (Cable, Transducer And Electrode, Patient, (Including Connector))
- Device class: 2
- Regulation: 21 CFR 870.2900
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K230571 (2023). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K230571: RFP-100A Connector Cable (Single Use), Baylis Medical Technologies, Inc. (2023) Summary page 5.

## Indications for use
The Baylis Connector Cable is intended to connect Baylis Radiofrequency (RF) Puncture Generators to separately cleared compatible RF devices.

Source page: https://510kreport.com/device/K254114
Methodology: https://510kreport.com/methodology