# K023674: Philips Drug Calculator Software

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems
- Decided: Nov 29, 2002 after 28 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
Longest line of descent: 5 generations back to K941811 (1994). 21 ancestors in all.
17 later devices descend from it; 1 cites it directly.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K922058: Models M1175A and M1176A Component Monitoring Syst, Hewlett-Packard Co. (1992) Summary page 1.
- K992636: HP Carevue 9000 Clinical Information System, Model M2331A, Hewlett-Packard Co. (1999) Summary page 1.
- K021422: Philips Information Center Software Revision D.02, Philips Medical Systems (2002)

## Most influential descendants
- K061110: Glucommander Plus (2006), 16 descendants of its own
- K101344: G+ System (2010), 13 descendants of its own
- K113853: G+ System (2012), 12 descendants of its own
- K132547: Endo Tool Glucose Management System (Egms) (2014), 8 descendants of its own
- K200443: EndoTool IV 1.10 (2020), 3 descendants of its own

## Indications for use
For central monitoring of adult, pediatric, and neonatal patients; and where the clinician decides to monitor cardiac arrhythmia of adult, pediatric, and neonatal patients and/or ST segment of adult patients to gain information for treatment, to monitor adequacy of treatment, or to exclude causes of symptoms.

Source page: https://510kreport.com/device/K023674
Methodology: https://510kreport.com/methodology