# K040084: Lifestyle Circulatory Enhancer

- Pathway: 510(k) (Abbreviated)
- Applicant: Advanced Circulatory Systems, Inc.
- Decided: Apr 7, 2004 after 83 days
- Product code: BWF (Spirometer, Therapeutic (Incentive))
- Device class: 2
- Regulation: 21 CFR 868.5690
- 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 K955138 (1995). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022906: Resqpod Circulatory Enhancer, Cprx, LLC (2003) Summary page 1.
- K033401: Modification to Resqpod Circulatory Enhancer, Advanced Circulatory Systems, Inc. (2003) Summary page 1.
- K032325: Jobst Travel Socks, Bsn-Jobst, Inc. (2003) Summary page 1.
- K951234: Medical Support Stockings, Jobst A Beiersdorf Co. (1995) Summary page 1.

## Indications for use
The Lifestyle Circulatory Enhancer (CE) is indicated for the temporary increase in blood circulation as prescribed by a physician or licensed practitioner. The Lifestyle CE may benefit people who suffer from states of poor circulation and low blood flow, including those individuals who suffer from orthostatic hypotension symptoms, such as lightheadedness, when moving from a sitting or reclining position to a standing position.

Source page: https://510kreport.com/device/K040084
Methodology: https://510kreport.com/methodology