# K890938: Kendall SCD Therapeutic System

- Pathway: 510(k) (Traditional)
- Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health
- Decided: May 19, 1989 after 84 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.
13 later devices descend from it; 5 cite it directly.
0 of 14 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
- K012403: Vanguard Reprocessed Compression Garment (2001), 3 descendants of its own
- K012008: STS Range , Models STS20,STS30,STS40 (2001), 3 descendants of its own
- K133119: Flowtron ACS800 Pump and Tri Pulse Garments (2014), 2 descendants of its own
- K031189: Uuhc Reprocessed Compression Sleeve Devices (2003), 2 descendants of its own
- K143438: Flowtron ACS900 (2015), 1 descendant of its own

Source page: https://510kreport.com/device/K890938
Methodology: https://510kreport.com/methodology