# K093658: Renu Medical Vasopress Calf , Thigh Garments- All Sizesd, Renu Medical Vasopress Foot Garments

- Pathway: 510(k) (Traditional)
- Applicant: Renu Medical, Inc.
- Decided: Jan 14, 2010 after 50 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: 3 generations back to K012417 (2002). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051227: Renu Medical Reprocessed Alp 1 Calf Garment, Model ALP1, Renu Medical, Inc. (2006) Summary page 1.

## Cited in the summary but kept off the family tree
- K031159: Calibrating Material, Calibrating Standards, Diamond Diagnostics, Inc. (2003). Our reading of the summary gave K031159, FDA’s number for Calibrating Material, Calibrating Standards (Diamond Diagnostics, Inc.). Its FDA name has none of the distinctive words the summary uses for the device it names, “ReNu Medical Reprocessed many different manufacturers types/sizes…”. Kept off the family tree. Summary page 1.

## Indications for use
The ReNu Medical Reprocessed Vaso Press CTC calf, thigh and foot DVT garments are to be used by patients in bath the home and institutional settings as a non-invasive therapeutic method to prevent deep vien thrombosis and resulting pulmonary embolism.

Source page: https://510kreport.com/device/K093658
Methodology: https://510kreport.com/methodology