# K131306: IC-1545-DL Multi Flo DVT Combo Intermittent Pneumatic Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Bio Compression Systems, Inc.
- Decided: Jul 22, 2013 after 76 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 K881632 (1988). 5 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061857: Model Multi-Flo IC-1545-KT/-F Intermittent Circulator, Bio Compression Systems, Inc. (2006) Summary page 4.

## Most influential descendants
- K180248: VascuEase IC-1200-WH (2018), 1 descendant of its own
- K232270: DVT Motion Pneumatic Compression Device (2024), 0 descendants of its own

## Indications for use
When used with GID-3045-T Calf/Thigh or GID-3045-K Calf garments: Intended for prophylaxis of deep vein thrombosis When used with GI-3045-F Foot Garments Intended for prophylaxis of deep vein thrombosis Enhancement of venous and arterial circulation Prevention of venous stasis ulcers Reduction of acute or chronic edema Reduction of lower limb pain due to surgery or trauma Reduction of compartment pressures

Source page: https://510kreport.com/device/K131306
Methodology: https://510kreport.com/methodology