# K072813: Emma Analyzer (Kpa & MMHG); Emma Monitor (Kpa & MMHG)

- Pathway: 510(k) (Traditional)
- Applicant: Phasein AB
- Decided: Dec 28, 2007 after 88 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: 4 generations back to K935370 (1994). 8 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K963327: Tidal Wave Carbon Dioxide Monitor, Model 610, Novametrix Medical Systems, Inc. (1996) Summary page 1.
- K063167: Emma Analyzer (Kpa) and (MMHG); Emma Monitor (Kpa) and (MMHG), Phasein AB (2007) Summary page 1.

## Most influential descendants
- K201590: EMMA Capnograph (2021), 0 descendants of its own

## Indications for use
The EMMA Emergency Capnometer Monitor measures, displays and monitors carbon dioxide concentration and respiratory rate during anesthesia, recovery and respiratory care. It may be used in the operating suite, intensive care unit, patient room, clinic, emergency medicine and emergency transport settings for adult, pediatric and infant patients. The EMMA Emergency Capnometer Analyzer measures and displays carbon dioxide concentration and respiratory rate during anesthesia, recovery and respiratory care. It may be used in the operating suite, intensive care unit, patient room, clinic, emergency medicine and emergency transport settings for adult, pediatric and infant patients.

Source page: https://510kreport.com/device/K072813
Methodology: https://510kreport.com/methodology