# K950835: Scimed Choice PT Ptca Guide Wire

- Pathway: 510(k) (Traditional)
- Applicant: Scimed Life Systems, Inc.
- Decided: May 25, 1995 after 90 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.
11 later devices descend from it; 1 cites it directly.
1 of 12 devices in its family (counting itself) has 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
- K970244: Scimed Choice Family of Ptca Guide Wires (1997), 10 descendants of its own
- K021363: Endovascular Guide Wire (2002), 8 descendants of its own
- K042854: Stereotaxis Endovascular Guide Wire (2005), 6 descendants of its own
- K052347: Titan Steerable (Ptca) Guidewire (2006), 2 descendants of its own
- K060454: Titan Guidewire (2006), 1 descendant of its own

Source page: https://510kreport.com/device/K950835
Methodology: https://510kreport.com/methodology