# K915092: Talley TM300 Sequential Multicom Compression Syst

- Pathway: 510(k) (Traditional)
- Applicant: Progressive Medical Technology, Inc.
- Decided: Feb 11, 1992 after 82 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.
35 later devices descend from it; 3 cite it directly.
0 of 36 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
- K993758: Proair 3000 Compression System (2000), 31 descendants of its own
- K060146: Activecare ++ System (2006), 30 descendants of its own
- K062818: Flexitouch System (2006), 10 descendants of its own
- K120972: Flexitouch System (2012), 9 descendants of its own
- K110159: Activecare SFT (2011), 9 descendants of its own

Source page: https://510kreport.com/device/K915092
Methodology: https://510kreport.com/methodology