# K083704: Nutrac Pelvator, Model Pel 200

- Pathway: 510(k) (Traditional)
- Applicant: Verity Scientific, Ltd.
- Decided: Jul 14, 2009 after 211 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.
12 later devices descend from it; 2 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K018148: Kegel8 Pelvic Muscle Trainer. Not in FDA’s 510(k), De Novo or PMA lists as we hold them (a misreading, a typo, or a number FDA does not list), so it is kept off the family tree Summary page 1.

## Most influential descendants
- K141643: Yarlap (2015), 10 descendants of its own
- K191312: Perfect PFE (2019), 3 descendants of its own
- K160773: Yarlap II (2016), 2 descendants of its own
- K260178: Pelvic Muscle Trainer (KM510, KM516B) (2026), 0 descendants of its own
- K252601: Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle Trainer (PC22E); Pelvic Muscle Trainer (PC22E-L) (2026), 0 descendants of its own

## Indications for use
The 'NuTraCTM Pelvator' Pelvic Muscle Trainer is intended to provide electrical stimulation and neuromuscular re-education for the purpose of rehabilitation of weak pelvic floor muscles for the treatment of stress urge and :mixed urinary incontinence in women

Source page: https://510kreport.com/device/K083704
Methodology: https://510kreport.com/methodology