# K030940: Nomad ND1000M Augmented Vision System

- Pathway: 510(k) (Traditional)
- Applicant: Microvision Incorporated
- Decided: Apr 9, 2003 after 15 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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 K923160 (1992). 4 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K961800: Head Mounted Display, Vista Medical Technologies, Inc. (1996) Summary page 1.
- K000669: Medivision I-View Personal Video Display, Medivision Endoscopy (2000) Summary page 2.

## Most influential descendants
- K040244: Microoptical's Critical Data Viewers, Models MD-3 and MD-6 (2004), 1 descendant of its own
- K042923: MD-6W Wireless Critical Data Viewer (2004), 0 descendants of its own

## Indications for use
The intended use of the NomadTMND1 OOOM system is to display video data or images while worn on the user's head.

Source page: https://510kreport.com/device/K030940
Methodology: https://510kreport.com/methodology