VersaCross RF Wire
FDA 510(k) K242076 · Baylis Medical Company
510(k) numberK242076
Submission
- Device name
- VersaCross RF Wire
- Applicant
- Baylis Medical Company
Mississauga, CA - Received
- July 16, 2024
- Decision date
- November 1, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DXF – Catheter, Septostomy
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.5175
- Specialty
- Cardiovascular
Other 510(k)s with product code DXF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261745 | LightningWire Transseptal Puncture System (TPS)DXF · Traditional | ElectroWire Medical | 06/26/2026SE |
| K253799 | SafeSept RF Transseptal Guidewire (SSRF132; SSRF132R; SSRF232; SSRF232R; SSRF135…DXF · Special | Pressure Products Medical Device Manufacturing… | 03/13/2026SE |
| K260292 | Hotwire RF Guidewire (901XXX); Hotwire RF Guidewire (902XXX)DXF · Special | Atraverse Medical | 02/27/2026SE |
| K252419 | Hotwire RF Guidewire (901XXX); Hotwire RF Guidewire (902XXX)DXF · Traditional | Atraverse Medical, Inc. | 08/27/2025SE |
| K251007 | CrossWise RF Transseptal Access System (Models: CW-1085S, CW-1085A, CW-1012W, CW-1012C…DXF · Special | Circa Scientific, Inc. | 05/01/2025SE |
| K243193 | Cross Wise Multi-Use RF Adapter CableDXF · Special | Circa Scientific, Inc. | 11/26/2024SE |
| K241414 | CrossWise RF Transseptal Access System (Models: CW-1085S, CW-1085A, CW-1012W, CW-1012C)…DXF · Traditional | Circa Scientific, Inc. | 09/26/2024SE |
| K240900 | HOTWIRE RF GuidewireDXF · Traditional | Atraverse Medical | 05/01/2024SE |
| K232852 | Cross Vascular RF Transseptal Needle, Cross Vascular Connection CableDXF · Traditional | Cross Vascular, Inc. | 10/12/2023SE |
| K221528 | Fogarty Dilation Atrioseptostomy Catheter, Miller Balloon Atrioseptostomy CatheterDXF · Traditional | Edwards Lifesciences, LLC | 08/22/2022SE |
More from Edwards Lifesciences, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K251325 | VersaCross Connect Transseptal DilatorDRE · Special | 05/29/2025SE |
| K241720 | VersaCross Connect Transseptal DilatorDRE · Special | 07/12/2024SE |
| K231227 | SureFlex HD Steerable Sheath, VersaCross HD Steerable SheathDYB · Traditional | 12/20/2023SE |
| K233647 | VersaCross Connect Transseptal DilatorDRE · Special | 12/14/2023SE |
| K213898 | ProTrack Pigtail WireDQX · Traditional | 03/01/2023SE |
| K221351 | Mechanical GuidewireDQX · Traditional | 12/19/2022SE |
| K213582 | Epicardial Access SystemDYB · Special | 06/30/2022SE |
| K220414 | VersaCross Connect Transseptal DilatorDYB · Special | 05/09/2022SE |
| K201288 | ExpanSure Large Access Transseptal DilatorDRE · Special | 06/12/2020SE |
| K191546 | Epicardial Access SystemDYB · Traditional | 08/02/2019SE |
Questions and answers
When was VersaCross RF Wire cleared by the FDA?
VersaCross RF Wire (K242076) received a 510(k) decision of Substantially Equivalent on November 1, 2024, 108 days after the submission was received.
What is the product code of K242076?
The FDA product code is DXF – Catheter, Septostomy, a Class II (moderate risk) device regulated under 21 CFR 870.5175.