# P880042: Edap LT.01 Shock Wave Lithotripter

- Pathway: PMA
- Applicant: Edap International Corp.
- Decided: Dec 12, 1991 after 1,288 days
- Product code: LNS (Lithotriptor, Extracorporeal Shock-Wave, Urological)
- Device class: 2
- Regulation: 21 CFR 876.5990
- 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. PMA decisions do not claim a predicate device.

## Most influential descendants
- K111808: Sonolith I-Move (2011), 0 descendants of its own

Source page: https://510kreport.com/device/P880042
Methodology: https://510kreport.com/methodology