# K882683: Jobst Extremity Pump (R) System 7500

- Pathway: 510(k) (Traditional)
- Applicant: Jobst Institute, Inc.
- Decided: Sep 20, 1988 after 82 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
No predicates in its family tree.
36 later devices descend from it; 7 cite it directly.
0 of 37 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
- K013331: Lympha Press Plus Device (2001), 26 descendants of its own
- 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

Source page: https://510kreport.com/device/K882683
Methodology: https://510kreport.com/methodology