# K984258: Neurovasx Sub-Microinfusion Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Neuro Vasx, Inc.
- Decided: Feb 11, 1999 after 73 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K862983 (1986). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K963988: Intravascular Infusion Device, Boston Scientific Corp (1996) Summary page 1.
- K964154: Segue Infusion Catheter, Interventional Innovations Corp. (1997) Summary page 1.
- K862983: Additional Target Therapeutics Guide Wires, Target Therapeutics (1986) Summary page 1.

## Most influential descendants
- K011646: Neuroedge Infusion  Catheter (2001), 0 descendants of its own

## Indications for use
The NeuroVasx Sub-Microinfusion Catheter is intended for the delivery of diagnostic agents into the neurovasculature.

Source page: https://510kreport.com/device/K984258
Methodology: https://510kreport.com/methodology