# K002297: Yoramed, Model T-202

- Pathway: 510(k) (Traditional)
- Applicant: United Yoram Distributors, Inc.
- Decided: Mar 15, 2001 after 230 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K030140: Duomed, Series 500, (Models ID 500, FL 500) (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K002297
Methodology: https://510kreport.com/methodology