# K093822: Docking Station,Teirstein Edge,Angioassist Combination Device, Angioassist Family

- Pathway: 510(k) (Traditional)
- Applicant: Shepherd Scientific, Inc.
- Decided: Jan 28, 2010 after 45 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
Longest line of descent: 5 generations back to K970376 (1997). 24 ancestors in all.
No later device cites it as a predicate yet.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K963171: Cinch QR SGW Extension, Cordis Corp. (1996) Summary page 1.
- K062192: Ostial Pro Stent Positioning System, Ostial Solutions, LLC (2007) Summary page 1.
- K072552: Merit Medical Systems, Inc., Guide Wire Torque Device, Merit Medical Systems, Inc. (2007) Summary page 1.
- K003398: Wireclip Torquer, Boston Scientific Corporation Northwest Technology (2000) Summary page 1.
- (no number) KEEP Accessory Organizer: named in the summary without a submission number

## Indications for use
The AngioAssist is a set of manual instruments intended to facilitate alignment and introduction of interventional devices (i.e., guide wires and catheters) within the coronary and peripheral vasculature.

Source page: https://510kreport.com/device/K093822
Methodology: https://510kreport.com/methodology