# K983052: Peritron Perineometer Model 9300V or 9300A

- Pathway: 510(k) (Traditional)
- Applicant: Cardio Design Pty., Ltd.
- Decided: Oct 19, 1998 after 48 days
- Product code: HIR (Perineometer)
- Device class: 2
- Regulation: 21 CFR 884.1425
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Contimed II™ (Hollister, Illinois): named in the summary without a submission number

## Most influential descendants
- K142355: Vaginal Tactile Imager (2015), 1 descendant of its own
- K231875: Vaginal Tactile Ultrasound Imager (2024), 0 descendants of its own

## Indications for use
Peritron is used in assessing the strength of pelvic floor muscles, teaching pelvic floor muscle exercises and for providing feedback during pelvic floor muscles exercises.

Source page: https://510kreport.com/device/K983052
Methodology: https://510kreport.com/methodology