# K002212: Mirage Hydrophilic Guidewire, Model 103-0608

- Pathway: 510(k) (Special)
- Applicant: Micro Therapeutics, Inc.
- Decided: Aug 3, 2000 after 13 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
38 later devices descend from it; 4 cite it directly.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K032146: PVS 1300 Synchro 0.014 & PVS 1600 Synchro 0.010 Guide Wires (2003), 28 descendants of its own
- K173235: Aristotle 14 Guidewire, 200cm, Soft Profile, Aristotle 14 Guidewire, 200cm, Support Profile, Aristotle 14 Guidewire, 300cm, Soft Profile, Aristotle 14 Guidewire, 300cm, Support Profile (2018), 16 descendants of its own
- K183608: Aristotle 18 Guidewire, 200cm, Soft Profile ; Aristotle 18 Guidewire, 200cm, Standard Profile ; Aristotle 18 Guidewire, 200cm, Support Profile (2019), 13 descendants of its own
- K192783: Aristotle 24 Guidewire, 200cm, Soft Profile ; Aristotle 24 Guidewire, 200cm, Standard Profile ; Aristotle 24 Guidewire, 200cm, Support Profile (2019), 12 descendants of its own
- K050964: PV 1900 Synchro 0.016 Guidewire (2005), 10 descendants of its own

Source page: https://510kreport.com/device/K002212
Methodology: https://510kreport.com/methodology