NZXClass II

Water, Vascular Access Flush

21 CFR 880.5200 / General Hospital

NZX is the FDA product code for Water, Vascular Access Flush, a class II device type, regulated under 21 CFR 880.5200. FDA's definition for this code reads: "Enhance the performance of intravascular catheters, to maintain patency of the vascular catheter when it is not in use". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: NZX
Device name: Water, Vascular Access Flush
FDA definition: Enhance the performance of intravascular catheters, to maintain patency of the vascular catheter when it is not in use.
Regulation: 21 CFR 880.5200
Device class: Class II
Review panel: General Hospital
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code NZX.

Recent clearances

Product code NZX

FDA records hold no clearances under product code NZX.

Recent recalls

Product code NZX

FDA records show no recalls under product code NZX.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)