# K010265: Baylis Medical RF Perforation Probe, Model RFP-265

- Pathway: 510(k) (Traditional)
- Applicant: Baylis Medical Co., Inc.
- Decided: Apr 9, 2001 after 73 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K051670: RF Tunneler Wire (2006), 6 descendants of its own
- K101615: Powerwire Radiofrequency Guidewire (2010), 2 descendants of its own
- K232562: PowerWire Radiofrequency Guidewire Kit (2024), 1 descendant of its own
- K101599: RVT Cto Device (2011), 1 descendant of its own
- K251158: PowerWire® 14 Radiofrequency Guidewire Kit (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K010265
Methodology: https://510kreport.com/methodology