# P840008: Dornier Lithotripter Compact Transportable (DLCT)

- Pathway: PMA
- Applicant: Dornier Medtech America, Inc.
- Decided: Dec 19, 1984 after 301 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.
34 later devices descend from it; 7 cite it directly.
0 of 35 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
- K011873: Dornier Lithotripter S (Doli S) & Dornier Lithotripter S-XP (Doli S-XP) (2001), 14 descendants of its own
- K040470: Tripter X-1 Compact (2004), 9 descendants of its own
- K041582: Modification to Tripter X-1 Compact Duet (2004), 8 descendants of its own
- K011773: Dornier Lithotripter 140(Doli 140) (2001), 7 descendants of its own
- K121656: Gemini Lithotripter (2012), 6 descendants of its own

Source page: https://510kreport.com/device/P840008
Methodology: https://510kreport.com/methodology