# K993826: Narkomed 6000

- Pathway: 510(k) (Traditional)
- Applicant: Draeger Medical, Inc.
- Decided: Mar 23, 2000 after 132 days
- Product code: MLC (Monitor, St Segment)
- Device class: 2
- Regulation: 21 CFR 870.2340
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K901713 (1990). 3 ancestors in all.
16 later devices descend from it; 1 cites it directly.
4 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K980553: Narkomed 6000 Model Number NM6000, Draeger Medical, Inc. (1998) Summary page 1.
- K921669: Marquette SL Series Transport Remote Acquisition, Marquette Electronics, Inc. (1993) Summary page 1.
- K901713: Narkomed 4 Anesthesia System, Draeger Medical, Inc. (1990) Summary page 1.

## Most influential descendants
- K033498: Narkomed 6400, Model NM6400 (2004), 15 descendants of its own
- K041622: Modification to Fabius GS Anesthesia System; Fabius Tiro Anesthesia System (2004), 14 descendants of its own
- K042607: Primus US (2004), 10 descendants of its own
- K142552: A7 Anesthesia System (2015), 5 descendants of its own
- K151954: A7 Anesthesia System (2015), 4 descendants of its own

## Indications for use
The NM6000 w/ CV & SCR in indicated as a continuous flow anesthesia system. The NM6000 w/ CV & SCR may be used for manually assisted, or automatic ventilation, and delivery of gases, anesthetic vapor, and monitoring of; oxygen concentration, breathing pressure, respiratory volume, cardiovascular parameters, anesthetic agent identification and concentration and provides printed data. Federal law restricts this device to sale by or on the order of a physician.

Source page: https://510kreport.com/device/K993826
Methodology: https://510kreport.com/methodology