# K002766: Nicolet Vasoguard

- Pathway: 510(k) (Abbreviated)
- Applicant: Nicolet Biomedical
- Decided: Nov 30, 2000 after 86 days
- Product code: JOP (Transducer, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 870.2880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 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
- K111416: Falcon (2011), 5 descendants of its own
- K131623: Smartdop XT (2014), 1 descendant of its own
- K242662: Falcon/Xpress (Falcon/Xpress) (2024), 0 descendants of its own
- K233976: VasoGuard (V10, V8, V6, V4, V2) (2024), 0 descendants of its own
- K153762: Smartdop XT6 (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K002766
Methodology: https://510kreport.com/methodology