# K080675: Pajunk Infiltralong Wound Infiltration Catheter Kit

- Pathway: 510(k) (Traditional)
- Applicant: PAJUNK GmbH Medizintechnologie
- Decided: Jun 20, 2008 after 102 days
- Product code: BSO (Catheter, Conduction, Anesthetic)
- Device class: 2
- Regulation: 21 CFR 868.5120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K813186 (1981). 8 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022869: Soaker Catheter, I-Flow Corp. (2002) Summary page 2.
- K051401: ON-Q Catheter, on-Antimicrobial Catheter, Soaker Catheter, I-Flow Catheter, I-Flow Corp. (2005) Summary page 2.

## Most influential descendants
- K111031: Painfusor Catheter (2011), 1 descendant of its own
- K193664: SubQKath Catheter and Needle Set (2020), 0 descendants of its own

## Indications for use
PAJUNK®'s Wound Infiltration Catheter Kit called InfiltraLong is intended for continuous or intemittent praeoperative, perioperative or post-operative delivery of local anesthetics or narcotics to wounds and surgical wound sites. Routes of administration may be intraoperative or percutaneous. The sterile components are available seperately.

Source page: https://510kreport.com/device/K080675
Methodology: https://510kreport.com/methodology