# K113819: Mongoose Angiographic Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Pediacath, Inc.
- Decided: Jul 11, 2012 after 197 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- 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 K960806 (1996). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K943739: Softouch Diagnostic Intravascular Catheter, Mallinckrodt Medical (1994) Summary page 2.
- K060116: Micrus Courier Microcatheters, Micrus Endovascular Corporation (2006) Summary page 2.

## Most influential descendants
- K171264: Royal Flush Catheter (2018), 0 descendants of its own

## Indications for use
The Mongoose Angiographic Catheter is intended for the delivery of contrast media to selected sites in the vascular system of adult and pediatric patients of all ages in conjunction with routine diagnostic procedures.

Source page: https://510kreport.com/device/K113819
Methodology: https://510kreport.com/methodology