# K082873: Medtronic Angiographic Guide Wires

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Vascular
- Decided: Feb 6, 2009 after 130 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: 1 generation back to K772021 (1977). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K772021: TRC Stainless Steel Safety Spring Guides, Usci, Div. C.R. Bard, Inc. (1977) Summary page 1.
- K780438: Safety Spring Guides, Teflon Coated, C.R. Bard, Inc. (1978) Summary page 1.

## Indications for use
The Medtronic Angiographic Guide Wires are indicated for percutaneous entry into vessel using the Seldinger technique.

Source page: https://510kreport.com/device/K082873
Methodology: https://510kreport.com/methodology