# K001917: Parodi Catheter for Angiography (Parca)

- Pathway: 510(k) (Traditional)
- Applicant: Arteria Medical Science, Inc.
- Decided: Jun 6, 2001 after 348 days
- Product code: MJN (Catheter, Intravascular Occluding, Temporary)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
14 later devices descend from it; 2 cite it directly.
2 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K070770: Gore Balloon Sheath (2007), 6 descendants of its own
- K023548: Proxis Flow-Control Device, Models Eps 101, IC 101 (2003), 6 descendants of its own
- K083300: Gore Flow Reversal System (2009), 5 descendants of its own
- K042117: Proxis System, Model Eps 101 (2005), 5 descendants of its own
- K060651: Proxis System, Model EPS101 (2006), 3 descendants of its own

Source page: https://510kreport.com/device/K001917
Methodology: https://510kreport.com/methodology