# K952536: SONO 5

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer Elektromedizin GmbH
- Decided: Mar 5, 1996 after 278 days
- Product code: IMI (Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat)
- Device class: 2
- Regulation: 21 CFR 890.5300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K121059: Soleoline, Soleo Stim, Soleo Sono, Soleo Sonostim (2012), 4 descendants of its own
- K161628: JAS Pulse (TM) Ultrasonic Therapy (2016), 3 descendants of its own
- K241099: Plasonic (Plasonic) (2024), 2 descendants of its own
- K260397: SYNERJET PRO (SP-1002); InPhiuse (SP-1002); WOWJET (SP-1002) (2026), 0 descendants of its own
- K251334: New Doublo 2.0 (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K952536
Methodology: https://510kreport.com/methodology