# K040584: NMX-1000

- Pathway: 510(k) (Traditional)
- Applicant: Neomedix Corp.
- Decided: Apr 22, 2004 after 48 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K792365 (1979). 16 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K024304: Microsurgical Bipolar Handpiece, Neomedix Corp. (2003) Summary page 1.
- (no number) Storz Goniotomy knife: named in the summary without a submission number

## Most influential descendants
- K220891: Kahook Dual Blade Glide (KDB Glide) (2024), 0 descendants of its own

## Indications for use
The NMX-1000 TM is designed to surgically remove a strip of the Trabecular meshwork for surgical management of infantile and aidult glaucoma.

Source page: https://510kreport.com/device/K040584
Methodology: https://510kreport.com/methodology