# K093920: Busse Epidural Catheter Kit

- Pathway: 510(k) (Traditional)
- Applicant: Busse Hospital Disposables
- Decided: Aug 6, 2010 after 227 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: 1 generation back to K001717 (2000). 1 ancestor in all.
2 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)
- K001717: Micor Conduction Catheter, Micor, Inc. (2000) Summary page 1.

## Most influential descendants
- K170900: DASH 6 NRFit Lock Syringe + Accessories, DASH 6 NRFit Slip Syringe + Accessories, DASH 6 NRFit Plastic LOR Syringe + Accessories (2017), 1 descendant of its own
- K201031: NRFit® Caps, Male and Female Neuraxial Tip Caps (2020), 0 descendants of its own

## Indications for use
The epidural catheter kit is intended for administration of local anesthetics into epidural space. Busse recommends the removal and/or replacement of the catheter every 72 hours.

Source page: https://510kreport.com/device/K093920
Methodology: https://510kreport.com/methodology