# K950349: Dynatron 950

- Pathway: 510(k) (Traditional)
- Applicant: Dynatronics Corp.
- Decided: Sep 13, 1995 after 229 days
- Product code: LIH (Interferential Current Therapy)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
38 later devices descend from it; 1 cites it directly.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K031329: Dynatron Solaris Series, Models 705, 706, 708, 709 D880 Infrared Probe (Optional Accessory) (2003), 37 descendants of its own
- K040729: Solaris D890 Therapy Probe (2004), 28 descendants of its own
- K043586: Laser Sys*Stim 540, Model ME 540 (2005), 13 descendants of its own
- K050070: K-Laser, Models 3,4,4D,6D (2005), 12 descendants of its own
- K113017: Sys*Stim 240 (2012), 9 descendants of its own

Source page: https://510kreport.com/device/K950349
Methodology: https://510kreport.com/methodology