# K944959: Amplatz Super Stiff Guidewire

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corp
- Decided: Nov 4, 1994 after 28 days
- Product code: OCY (Endoscopic Guidewire, Gastroenterology-Urology)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K093515: 3 Piece Parodi Guidewire System ( Long Cut Outer with Long Taper .014) Short Taper, 2 Piece Parodi Guidewire System (Lon (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K944959
Methodology: https://510kreport.com/methodology