# K072422: Cyberwand Sterile Pads, Model: CW-Rbpbx

- Pathway: 510(k) (Special)
- Applicant: Cybersonics, Inc.
- Decided: Oct 24, 2007 after 57 days
- Product code: FFK (Lithotriptor, Electro-Hydraulic)
- Device class: 2
- Regulation: 21 CFR 876.4480
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K132795: Cyberwand Sterile Probe Set (2013), 0 descendants of its own

## Indications for use
The CyberWandTM Lithotripter with STERILE Probes is intended to be used for the intracorporeal fragmentation of urinary tract calculi in the kidney, ureter, bladder and biliary tracts.

Source page: https://510kreport.com/device/K072422
Methodology: https://510kreport.com/methodology