# K041956: Emg - Essential Gas Module, Model M1013A

- Pathway: 510(k) (Special)
- Applicant: Draeget Medical AG & Co. Kgaa
- Decided: Aug 9, 2004 after 19 days
- Product code: CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase)
- Device class: 2
- Regulation: 21 CFR 868.1400
- 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 K946306 (1995). 28 ancestors in all.
251 later devices descend from it; 2 cite it directly.
0 of 280 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012139: Vamos Anesthetic Gas Monitor, Draeger Medical, Inc. (2002) Summary page 2.
- K040847: Modification to Vamos Anesthetic Gas Monitor, Draeger Medical, Inc. (2004) Summary page 2.
- K031340: Siemens Infinity Modular Monitors, Models SC 8000, SC 7000 and SC 9000XL, with Scio, Siemens Medical Solutions USA, Inc. (2003) Summary page 2.
- K040917: Philips Anesthesia Gas Monitor, Model M1026B, Philips Medizin Systeme Boeblingen GmbH (2004) Summary page 2.

## Most influential descendants
- K050762: Philips Intellivue Patient Monitor, Models MP20, MP30, MP40, MP50, MP60, MP70 and MP90 (2005), 249 descendants of its own
- K051106: The Philips MP20, MP30, MP40, MP50, MP60, MP70, MP80 and MP90 Intellivue Patient Monitors (2005), 247 descendants of its own
- K052801: Intellivue Patient Monitors with Release C.02, Models MP20, MP30, MP40, MP50, MP60, MP70, MP80 and MP90 (2005), 234 descendants of its own
- K053522: Philips MP40, MP50, MP60, MP70, MP80 and MP90 Intellivue Patient Monitors, Release D.00 (2006), 233 descendants of its own
- K060221: The Phillips, Model MP20,MP30,MP40,MP50,MP60,MP70,MP80,and MP90 Intellivue Patient Monitors (2006), 222 descendants of its own

## Indications for use
The EGM gas monitor is indicated for measuring and monitoring C02 concentration and the concentrations of N20, 02, Halothane, Enflurane, Isoflurane, Sevoflurane and Desfiurane. Federal Law restricts this device to sale by or on the order of a physician.

Source page: https://510kreport.com/device/K041956
Methodology: https://510kreport.com/methodology