# K001120: Envoy Patient Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Mennen Medical, Ltd.
- Decided: May 8, 2001 after 396 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 4 cite it directly.
0 of 10 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
- K011784: Modification to Envoy Patient Monitor (2001), 3 descendants of its own
- K052288: Vitalogik (2005), 2 descendants of its own
- K030722: Envoy Patient Monitor (2004), 1 descendant of its own
- K141441: Menntor X7 (2015), 0 descendants of its own
- K073140: Vitalogik Model 4000/4500 (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K001120
Methodology: https://510kreport.com/methodology