# K070150: Vascupuncture Picc Guidewire

- Pathway: 510(k) (Special)
- Applicant: Neometrics, Inc.
- Decided: Feb 15, 2007 after 30 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 K011084 (2001). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031652: Vascupuncture Picc Guidewire, Neometrics, Inc. (2003) Summary page 1.
- K040786: Vascupuncture Picc Guidewire with Hydro-Silk Coating, Neometrics, Inc. (2004) Summary page 1.
- K043398: Modification to Vascupuncture Picc Guidewire, Neometrics, Inc. (2005) Summary page 1.

## Most influential descendants
- K101729: Neowire Pta/Ptca Guidewire (2010), 0 descendants of its own

## Indications for use
The VascuPuncture PICC Guidewire is indicated for percutaneous entry of peripheral vessels using the Seldinger Technique. The device is not intended for use in the coronary or cerebral vasculature.

Source page: https://510kreport.com/device/K070150
Methodology: https://510kreport.com/methodology