# K022404: Actiband

- Pathway: 510(k) (Traditional)
- Applicant: Paw, LLC
- Decided: Aug 8, 2002 after 16 days
- Product code: ILX (Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat)
- Device class: 2
- Regulation: 21 CFR 890.5290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K152432: ActiPatch (R) (2017), 1 descendant of its own
- K192234: ActiPatch (2020), 0 descendants of its own
- K190251: RecoveryRx (2019), 0 descendants of its own

## Indications for use
For the treatment of edema following Blepharoplasty

Source page: https://510kreport.com/device/K022404
Methodology: https://510kreport.com/methodology