# K944860: Scholar Patient Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Criticare Systems, Inc.
- Decided: Jun 20, 1995 after 260 days
- Product code: MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms))
- 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.
22 later devices descend from it; 2 cite it directly.
1 of 23 devices in its family (counting itself) has 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
- K012059: 8100/8500 Vital Signs Monitor (2001), 15 descendants of its own
- K093261: MOVES (2010), 7 descendants of its own
- K022435: 507EL Vital Signs Monitor (2002), 6 descendants of its own
- K141460: Finapres Nova Noninvasive Hemodynamic Monitor (2015), 4 descendants of its own
- K051038: 506 Patient Monitor (2005), 4 descendants of its own

Source page: https://510kreport.com/device/K944860
Methodology: https://510kreport.com/methodology