# K974395: Atlant's

- Pathway: 510(k) (Traditional)
- Applicant: Grad-Line Corp.
- Decided: Oct 22, 1998 after 335 days
- Product code: IRP (Massager, Powered Inflatable Tube)
- Device class: 2
- Regulation: 21 CFR 890.5650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K053225: Cellu M6 Keymodule I (2006), 3 descendants of its own
- K092734: E-Light Line (2010), 2 descendants of its own
- K124064: Young Again (2013), 1 descendant of its own
- K162556: Lightfusion Led System (2017), 0 descendants of its own

## Indications for use
For the treatment of chronic venous insufficiency, lymphedema, edema of venous origin, post amputation, lymphatic obstruction and contusions.

Source page: https://510kreport.com/device/K974395
Methodology: https://510kreport.com/methodology