← FDA DEVICE PRODUCT CODES
FDA PRODUCT CODE · CLASS II
NZX — Water, Vascular Access Flush
Enhance the performance of intravascular catheters, to maintain patency of the vascular catheter when it is not in use.
DEVICE CLASS
Class II
REGULATION
21 CFR 880.5200
MEDICAL SPECIALTY
General Hospital
REVIEW PANEL
HO
— Implant— Life-sustaining— GMP-exempt— Third-party review eligible
0
510(K)/PMA CLEARANCES
0
RECALL ENTRIES
Related on SPEQ
Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.
Weekly Briefing
Read a past issue →Get the Weekly GxP Briefing
Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.