# K052844: Kavs - Catheter, Models 1107100 & 1107060

- Pathway: 510(k) (Traditional)
- Applicant: Richter & Rothe AG
- Decided: Mar 20, 2006 after 164 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
Longest line of descent: 5 generations back to K904788 (1990). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041517: Infusioncath, Id, LLC (2004) Summary page 1.
- K002286: Ldob Occlusion Balloon Catheter, Cook, Inc. (2001) Summary page 1.

## Indications for use
The KAVS Catheter is intended to temporarily inhibit blood flow in isolated sections of peripheral veins in order to inject physician prescribed medications.

Source page: https://510kreport.com/device/K052844
Methodology: https://510kreport.com/methodology