# K093259: ARP RX100

- Pathway: 510(k) (Traditional)
- Applicant: Arp Manufacturing, Inc.
- Decided: Dec 17, 2009 after 59 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- 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 K893851 (1989). 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)
- K893851: Therastim, Physiodynamics, Inc. (1989) Summary page 1.

## Indications for use
The ARP RxlOO0 is indicated for the following applications: Relaxation of muscle spasms prevention or retardation of disuse atrophy Increasing local blood circulation Muscle re-education Maintaining or increasing range of motion

Source page: https://510kreport.com/device/K093259
Methodology: https://510kreport.com/methodology