# K051227: Renu Medical Reprocessed Alp 1 Calf Garment, Model ALP1

- Pathway: 510(k) (Traditional)
- Applicant: Renu Medical, Inc.
- Decided: Apr 7, 2006 after 330 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: 2 generations back to K012417 (2002). 8 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031559: Renu Medical Reporcessed Compressible Limb Sleeves, Renu Medical, Inc. (2003) Summary page 1.

## Most influential descendants
- K093658: Renu Medical Vasopress Calf , Thigh Garments- All Sizesd, Renu Medical Vasopress Foot Garments (2010), 0 descendants of its own
- K080551: University Health Care Processed Alternating Leg Pressure (Uhc Apl) Sleeve Device (2008), 0 descendants of its own

## Indications for use
The ReNu Medical Reprocessed ALP®1 is to be used by patients in both the home and institutional settings as a non-invasive therapeutic method to: * Prevent deep vein thrombosis and resulting pulmonary embolism.

Source page: https://510kreport.com/device/K051227
Methodology: https://510kreport.com/methodology