# K792354: The Circulator Boot

- Pathway: 510(k) (Traditional)
- Applicant: Circulator Boot Corp.
- Decided: Jan 9, 1980 after 50 days
- Product code: DRN (Device, Counter-Pulsating, External)
- Device class: 2
- Regulation: 21 CFR 870.5225
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K971026: The Circulator Boot (1997), 1 descendant of its own
- K082134: Circulator Boot (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K792354
Methodology: https://510kreport.com/methodology