# K240348: Quantum Mitohormesis (QMT) (M2101)

- Pathway: 510(k) (Abbreviated)
- Applicant: Quantumtx Pte., Ltd.
- Decided: Dec 19, 2024 after 318 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K940301 (1994). 28 ancestors in all.
No later device cites it as a predicate yet.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151834: BEMER Classic Set, BEMER Pro-Set, Bemer Int AG (2017) Summary page 5.
- K203710: Storz Medical MAGNETOLITH Muscle Stimulator, Storz Medical AG (2021) Summary page 5.

## Indications for use
Quantum Mitohormesis Medical Device is intended for: Stimulating healthy limb muscles to improve and facilitate muscle performance. Preventing or retardation of disuse atrophy of muscles.

Source page: https://510kreport.com/device/K240348
Methodology: https://510kreport.com/methodology