# K081697: The Wand Microaccess Safety Introducer, Models 90001, 90002, 90005, 90006

- Pathway: 510(k) (Traditional)
- Applicant: Access Scientific, Inc.
- Decided: Dec 4, 2008 after 170 days
- Product code: DYB (Introducer, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1340
- 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 K932323 (1993). 6 ancestors in all.
27 later devices descend from it; 2 cite it directly.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K840455: Emergency Infusion Device, Arrow Intl., Inc. (1984) Summary page 1.
- K020834: BD Introsyte Precision Introducer; BD Introsyte-N Precision Introducer; BD Introsyte Autoguard Shielded Introducer; BD I, Becton Dickinson Infusion Therapy Systems, Inc. (2002) Summary page 1.
- K071574: Stiffer Coaxial Micro-Introducer Kit, Enpath Medical, Inc. (2007) Summary page 1.

## Most influential descendants
- K101422: The Power Wand Safety Introducer with an Extended Dwell Catheter (2011), 25 descendants of its own
- K121073: Powerglide Midline Catheter (2012), 19 descendants of its own
- K133856: Powerglide Midline Catheter (2014), 12 descendants of its own
- K153280: PowerGlide Pro Midline Catheter (2016), 5 descendants of its own
- K150407: BioFlo Midline Catheter (2015), 5 descendants of its own

## Indications for use
The WAND TM MicroAccess Safety Introducer is used to facilitate the placing of an intravascular catheter through the skin into the peripheral circulatory system.

Source page: https://510kreport.com/device/K081697
Methodology: https://510kreport.com/methodology