# K061984: Treasure

- Pathway: 510(k) (Traditional)
- Applicant: Asahi Intecc Co., Ltd.
- Decided: Oct 5, 2006 after 84 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: 4 generations back to K890505 (1989). 15 ancestors in all.
32 later devices descend from it; 7 cite it directly.
3 of 48 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033742: Boston Scientific V-18 Control Wire, Boston Scientific Corp (2004). Our reading of the summary gave K033724, FDA’s number for Nobel Biocare Centric Post, Models 31234, 31235 and 31236 (Nobel Biocare Uas, Inc.). Corrected to the number with two digits swapped whose FDA name carries the summary’s words for the device, “Boston Scientific V-18 guide wire”.
- K982876: HI-Torque Steelcore 18 Guide Wire Model Numbers 1003280, 1003281, 1003282, Guidant Corp. (1998) Summary page 1.
- K022762: Jowire Neo's Ptca Catheter Guidewires, Models AG141000, AG142000, AG143000, AG141002, AG141010, AG14M060 & AG14M050, Jomed, Inc. (2002) Summary page 1.

## Most influential descendants
- K071721: Asahi Astato 30 Peripheral Guide Wire, Models - PAGH18M071, PAGH18M371 (2007), 27 descendants of its own
- K103057: Asahi Astato XS 20 Peripheral Guide Wire (2010), 21 descendants of its own
- K083146: Asahi Regalia XS 1.0 Peripheral Guide Wire, Models Pagp 140000 & Pagp 1403000 (2008), 17 descendants of its own
- K150445: ASAHI Peripheral Guide Wire Series (ASAHI Gladius, ASAHI Halberd, ASAHI Gaia PV) (2015), 16 descendants of its own
- K153443: ASAHI Astato XS 40 (2016), 14 descendants of its own

## Indications for use
The ASAHI Treasure guide wire is intended to facilitate the placement and exchange of diagnostic and therapeutic devices during intravascular procedures. This device is intended for peripheral vascular use only.

Source page: https://510kreport.com/device/K061984
Methodology: https://510kreport.com/methodology