# K072316: Precious Plus Guide Catheter

- Pathway: 510(k) (Special)
- Applicant: Asahi Intecc Co., Ltd.
- Decided: Sep 17, 2007 after 31 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
Longest line of descent: 3 generations back to K010874 (2001). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061601: Asahi Precious Guide Catheter, Asahi Intecc Co., Ltd. (2006) Summary page 1.
- K972484: Acs Viking Guiding Catheter, Guidant Corp. (1997) Summary page 1.

## Indications for use
The Precious Plus Guide Catheter is intended for use in coronary artery applications and is designed to provide a pathway through which medical instruments, such as balloon catheters, guide wires or other therapeutic devices may be introduced. These devices are not intended for use in the cerebral vasculature.

Source page: https://510kreport.com/device/K072316
Methodology: https://510kreport.com/methodology