# K932835: Kendall T.E.D./SCD Sequential Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health
- Decided: Aug 6, 1993 after 57 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K012403: Vanguard Reprocessed Compression Garment (2001), 3 descendants of its own
- K051438: Vanguard Reprocessed Compression Garments (Hill-Rom) (2006), 1 descendant of its own
- K100909: Reprocessed Compression Sleeves (2010), 0 descendants of its own
- K052691: Suretek Medical Reprocessed Compression Sleeves (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K932835
Methodology: https://510kreport.com/methodology