# K092117: Scenar, Model 10

- Pathway: 510(k) (Traditional)
- Applicant: Ritm Okb Zao
- Decided: May 28, 2010 after 318 days
- Product code: GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief)
- 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
Longest line of descent: 3 generations back to K951951 (1996). 4 ancestors in all.
1 later device descends 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)
- K042912: INTERX5000, Neuro Resource Group, Inc. (2005) Summary page 1.

## Most influential descendants
- K131513: Scenar (Scelap, Enisar, Ipens) Cutaneous Electrode Family (2014), 0 descendants of its own

## Indications for use
For relief and management of chronic and acute pain, as adjunctive treatment in the management of post-surgical and post-traumatic pain.

Source page: https://510kreport.com/device/K092117
Methodology: https://510kreport.com/methodology