# K001775: Zoe Medical Nightingale Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Zoe Medical, Inc.
- Decided: Jan 12, 2001 after 214 days
- Product code: DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
14 later devices descend from it; 3 cite it directly.
0 of 15 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
- K062144: Escort M8 Vital Signs Patient Monitor, Model 3810 (2006), 11 descendants of its own
- K090556: Spacelabs Elance Vital Signs Monitoring System and Central Monitor Software (2009), 10 descendants of its own
- K130740: Nightingale Monitoring System (2013), 3 descendants of its own
- K123556: Mortara Surveyor Patient Monitor (2013), 2 descendants of its own
- K161517: Mortara Surveyor Patient Monitor (2017), 1 descendant of its own

Source page: https://510kreport.com/device/K001775
Methodology: https://510kreport.com/methodology