# K992079: Kendall Model 7325 SCD Response Compression System, Model 7325

- Pathway: 510(k) (Special)
- Applicant: The Kendall Company, L.P.
- Decided: Sep 29, 1999 after 100 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.
42 later devices descend from it; 3 cite it directly.
0 of 43 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Kendall SCD Sequel™ Compression System: named in the summary without a submission number

## Most influential descendants
- K040511: SCD Express Portable Compression System (2004), 38 descendants of its own
- K102737: Kendall SCD 700 Sequential Compression Controller (2010), 11 descendants of its own
- K112677: The Venous Assist System (2012), 10 descendants of its own
- K110977: Vesoflow (2011), 6 descendants of its own
- K120944: Kendall SCD 700 Sequential Compression Controller (2012), 5 descendants of its own

## Indications for use
The SCD RESPONSE Compression System is designed to apply sequential compression to the lower Limbs to help prevent deep vein thrombosis in patients at risk.

Source page: https://510kreport.com/device/K992079
Methodology: https://510kreport.com/methodology