# K931574: Advance Model Uds-Adv

- Pathway: 510(k) (Traditional)
- Applicant: Laborie Medical Technologies, Ltd.
- Decided: Aug 5, 1993 after 128 days
- Product code: EXQ (Cystometer, Electrical Recording)
- Device class: 2
- Regulation: 21 CFR 876.1620
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 1 cites it directly.
0 of 12 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
- K073552: Laborie Urodynamic System with Tetra Accessory (2008), 10 descendants of its own
- K082701: Uronirs, Model 2000 (2008), 8 descendants of its own
- K120088: Mcompass Anorectal Manometry System (2012), 7 descendants of its own
- K161785: THD Anopress (2017), 4 descendants of its own
- K180135: THD Anopress with THD SensyProbe (2018), 3 descendants of its own

Source page: https://510kreport.com/device/K931574
Methodology: https://510kreport.com/methodology