# K872040: Phoresor II (TM), Model PM700

- Pathway: 510(k) (Traditional)
- Applicant: Motion Control, Inc.
- Decided: Aug 4, 1987 after 69 days
- Product code: EGJ (Device, Iontophoresis, Other Uses)
- Device class: 2
- Regulation: 21 CFR 890.5525
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K031769: E-Strip (2003), 0 descendants of its own
- K991991: Dupel Iontophoresis System (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K872040
Methodology: https://510kreport.com/methodology