# K071878: Delta Scanner, Delta Scanner Pro, DS Spine Pro, DS Sports Pro and DS Rehab

- Pathway: 510(k) (Traditional)
- Applicant: Med-Lectric Corporation
- Decided: Dec 7, 2007 after 154 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: 4 generations back to K951951 (1996). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 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.
- K053626: INTERX500 Flexible Array Electrode, Neuro Resource Group, Inc. (2006) Summary page 1.
- K062641: Body-Stim, Biomodulator, Best-Rsi, Best Pro, Model Best-AV1, Avazzia, Inc. (2007) Summary page 1.

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

Source page: https://510kreport.com/device/K071878
Methodology: https://510kreport.com/methodology