# K981413: Schneider Guider Softip Guiding Catheters

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific Scimed, Inc.
- Decided: May 13, 1998 after 23 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) SCHNEIDER GUIDER® Softip® guiding catheters: named in the summary without a submission number

## Indications for use
The SCHNEIDER GUIDER® Softip® Guiding Catheter is designed for the intravascular introduction of interventional devices.

Source page: https://510kreport.com/device/K981413
Methodology: https://510kreport.com/methodology