# K020637: Select Stim

- Pathway: 510(k) (Traditional)
- Applicant: Care Rehab and Orthopaedic
- Decided: May 28, 2002 after 90 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: 2 generations back to K840346 (1984). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K971542: Ortho DX Neuromuscular Stimulator, Rehabilicare, Inc. (1997) Summary page 1.

## Indications for use
The Select Stim is recommended for use for the following conditions: Relaxation of muscle spasms Prevention or retardation of disuse atrophy Increasing local blood circulation Muscle re-education Immediate post-surgical simulation of calf muscles to prevent venous thrombosis Maintaining or increasing range of motion

Source page: https://510kreport.com/device/K020637
Methodology: https://510kreport.com/methodology