# K013331: Lympha Press Plus Device

- Pathway: 510(k) (Traditional)
- Applicant: Mego Afek
- Decided: Nov 30, 2001 after 56 days
- Product code: JOW (Sleeve, Limb, Compressible)
- Device class: 2
- Regulation: 21 CFR 870.5800
- 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 K810338 (1981). 2 ancestors in all.
26 later devices descend from it; 6 cite it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K810338: Lympha Press, Mego Afek (1981) Summary page 1.
- K882683: Jobst Extremity Pump (R) System 7500, Jobst Institute, Inc. (1988) Summary page 1.
- (no number) Sequential Circulator device: named in the summary without a submission number

## Most influential descendants
- K082149: Lympha Press Optimal, Model# 1201AP (2008), 17 descendants of its own
- K100677: Lympha Press 201MAX, Model 201MAX (2010), 14 descendants of its own
- K123647: Circuflow 5208 Sequential Compression Device (2013), 12 descendants of its own
- K102320: Compressible Limb and Circulation Therapy System Model LX7(V7) (2011), 6 descendants of its own
- K131420: Petite Basic System 701 Elt (2013), 5 descendants of its own

## Indications for use
Treatment of Lymphatic Disorders, Venous Disorders, Post-mastectomy Lymphedema and Dysfunction of the “Muscle Pump”.

Source page: https://510kreport.com/device/K013331
Methodology: https://510kreport.com/methodology