# K100862: Bodyflow P2CH

- Pathway: 510(k) (Traditional)
- Applicant: Physiomed Elektromedizin AG
- Decided: Apr 21, 2011 after 388 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 K003896 (2002). 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)
- K003896: Lympha Vision-Expert, Bexley Trading, Inc. (2002) Summary page 1.

## Indications for use
The Bodyflow®-P2CH is a powered muscle stimulator intended for * Increased local blood circulation * Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis

Source page: https://510kreport.com/device/K100862
Methodology: https://510kreport.com/methodology