# K073082: CPS Courier Guidewire

- Pathway: 510(k) (Special)
- Applicant: Brivant, Ltd.
- Decided: Jan 9, 2008 after 69 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.
28 later devices descend from it; 4 cite it directly.
5 of 29 devices 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) Brivant Guidewire: named in the summary without a submission number

## Most influential descendants
- K081187: Bridgepoint Medical Entera Percutaneous Coronary and Peripheral Guidewire, Model M-3001 (2008), 13 descendants of its own
- K083727: Stingray Guidewire, Stiff, Models M-3003, M-3004, M-3011, M-3012 (2009), 12 descendants of its own
- K102725: Crossboss Catheter Model M-2000, Stingray Orienting Balloon Catheter Model M-1000, Stingray Guidewire Model M-3004 and M (2011), 11 descendants of its own
- K120298: CPS Excel Mediguide Enabled Guidewire (2012), 8 descendants of its own
- K190106: Intra-Operative Positioning System; Simple Curve Catheter, Reverse Curve Catheter ; Angled Tip Guidewire ; Tracking Pad ; Guidewire Handle (2019), 6 descendants of its own

## Indications for use
The CPS Courier Guidewires are intended for use in the coronary and peripheral vasculature.

Source page: https://510kreport.com/device/K073082
Methodology: https://510kreport.com/methodology