# K981344: Uresil Percutaneous Drainage Catheters with Hydrophilic Coating

- Pathway: 510(k) (Traditional)
- Applicant: Uresil Corp.
- Decided: Sep 10, 1998 after 154 days
- Product code: LJE (Catheter, Nephrostomy)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K063733: Resolve Biliary Drainage Catheter (2007), 2 descendants of its own
- K121832: Resolve Biliary Locking Drainage Catheter (2012), 1 descendant of its own
- K141408: Resolve Biliary Locking Drainage Catheter (2014), 0 descendants of its own

## Indications for use
For percutaneous drainage of abscess, nephrostomy and other fluids.

Source page: https://510kreport.com/device/K981344
Methodology: https://510kreport.com/methodology