# K930530: Incare PRS 9300 Pelvic FL Thera Syst/Treat Uri Inc

- Pathway: 510(k) (Traditional)
- Applicant: Hollister, Inc.
- Decided: Oct 17, 1995 after 987 days
- Product code: KPI (Stimulator, Electrical, Non-Implantable, For Incontinence)
- Device class: 2
- Regulation: 21 CFR 876.5320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
67 later devices descend from it; 7 cite it directly.
0 of 68 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K961872: Incare Pelvic Floor Therapy System with Desktop Computer (1996), 46 descendants of its own
- K974048: Incare Pelvic Floor Therapy System with Desktop Computer (1997), 42 descendants of its own
- K023906: Pathway CTS2000 Pelvic Floor Training System (2003), 39 descendants of its own
- K013612: Incare Pelvic Floor Therapy System (2002), 38 descendants of its own
- K050483: Evadri Bladder Control Systems (2005), 37 descendants of its own

Source page: https://510kreport.com/device/K930530
Methodology: https://510kreport.com/methodology