# K041772: Datex-Ohmeda Prestn.01 Module (Model Family M-Prestn.01) and Accessories

- Pathway: 510(k) (Special)
- Applicant: Datex-Ohmeda
- Decided: Jul 28, 2004 after 27 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.
18 later devices descend from it; 2 cite it directly.
2 of 19 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
- K043551: Datex-Ohmeda S/5 PSM Module, (Consisting of E-PSM and E-PSMP Modules) and Accessories (2005), 15 descendants of its own
- K062576: Datex-Ohmeda S/5 E-PSM (P) Module (Consisting of E-PSM, E-PSMP and E-Intpsm Modules) and Accessories (2006), 14 descendants of its own
- K120598: Procare Monitor B40 (2012), 10 descendants of its own
- K130584: Monitor B40 (2013), 8 descendants of its own
- K133576: Monitor B40 (2014), 7 descendants of its own

Source page: https://510kreport.com/device/K041772
Methodology: https://510kreport.com/methodology