# K915638: Talley TM200 Intermttent Compression Unit

- Pathway: 510(k) (Traditional)
- Applicant: Progressive Medical Technology, Inc.
- Decided: Feb 11, 1992 after 56 days
- Product code: IRP (Massager, Powered Inflatable Tube)
- Device class: 2
- Regulation: 21 CFR 890.5650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
48 later devices descend from it; 3 cite it directly.
0 of 49 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K022340: Travelair Portable Compression System (2003), 31 descendants of its own
- K061125: Dvtcare CA5 (2006), 30 descendants of its own
- K103187: Tripleplay-VT Vascular Therapy System (2011), 25 descendants of its own
- K133274: Vena Pro (2014), 22 descendants of its own
- K080134: Compressible Limb and Circulation Therapy System, Model WHF-314 (Power-Q1000) (2009), 14 descendants of its own

Source page: https://510kreport.com/device/K915638
Methodology: https://510kreport.com/methodology