# K950534: Scimed Sceptor Ptca Guide Wire

- Pathway: 510(k) (Traditional)
- Applicant: Scimed Life Systems, Inc.
- Decided: Apr 28, 1995 after 80 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.
3 later devices descend from it; 3 cite it directly.
0 of 4 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
- K965023: Choice PT Plus Ptca Guide Wire and Choice PT Vision Ptca Guide Wire (1997), 2 descendants of its own
- K974241: Scimed Informer Pressure Wire System (1998), 0 descendants of its own
- K980360: Scimed Quest Floppy and Moderate Support Guide Wires (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K950534
Methodology: https://510kreport.com/methodology