# K240358: ShockPhysio Mobile (model SW3200 Basic)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Dongdixin Technology Co., Ltd.
- Decided: Jun 5, 2024 after 120 days
- Product code: ISA (Massager, Therapeutic, Electric)
- Device class: 1
- Regulation: 21 CFR 890.5660
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The ShockPhysio Mobile (model SW3200 Basic) is indicated for: • Relief of minor muscle aches and pains • Temporary increase in local blood circulation • Activation of connective tissue

Source page: https://510kreport.com/device/K240358
Methodology: https://510kreport.com/methodology