# K913184: MS-Iii Ministim

- Pathway: 510(k) (Traditional)
- Applicant: Life-Tech Intl., Inc.
- Decided: Oct 7, 1991 after 81 days
- Product code: BXN (Stimulator, Nerve, Battery-Powered)
- Device class: 2
- Regulation: 21 CFR 868.2775
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K121743: Easymed Peripheral Nerve Stimulator-Sunstin (2013), 1 descendant of its own
- K153045: SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator (2016), 0 descendants of its own
- K143095: MiniStim MS-IVB Peripheral Nerve Stimulator (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K913184
Methodology: https://510kreport.com/methodology