# K141609: Pulstar Logix Pump

- Pathway: 510(k) (Special)
- Applicant: Albahealth, LLC
- Decided: Jul 15, 2014 after 29 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K142728: ActiveCare+SFT; ActiveCare+SFT HomeCare (ActiveCare+SFT-sub-category), ActiveCare+DTx ; ActiveCare+DTx HomeCare (ActiveCare+DTx-sub-category) (2014), 2 descendants of its own
- K151377: ActiveCare+SFT;ActiveCare+SFT HomeCare, ActiveCare+DTx;ActiveCare+DTx HomeCare (2015), 1 descendant of its own
- K160431: ActiveCare Home (2016), 0 descendants of its own

## Indications for use
Patients at Risk for DVT: These include: a. Major orthopedic procedures e.g. knee surgery Major abdominal thoracic surgery including urogenital surgery Neurosurgery, subarachnoid hemorrhage and stroke Bedridden Medical patients b. Patients with chronic venous insufficiency

Source page: https://510kreport.com/device/K141609
Methodology: https://510kreport.com/methodology