# K202044: Powerpress Recovery Unit

- Pathway: 510(k) (Traditional)
- Applicant: Hanuri Distribution, Inc.
- Decided: Oct 21, 2020 after 90 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
Longest line of descent: 1 generation back to K112479 (2011). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112479: DSJ Massager, Mego Afek AC, Ltd. (2011) Summary page 4.

## Indications for use
The Powerpress Recovery Unit is indicated for the temporary relief of minor muscle aches and pains, and for temporary increase in circulation to the treated areas in people who are in good health. The Powerpress Recovery Unit simulates kneading and stroking of tissues by using an inflatable garment.

Source page: https://510kreport.com/device/K202044
Methodology: https://510kreport.com/methodology