# K031600: Conduction Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Micor, Inc.
- Decided: Aug 13, 2003 after 84 days
- Product code: FRN (Pump, Infusion)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K885278 (1989). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K991879: Spring-Wound Epidural Catheter, Micor, Inc. (1999) Summary page 1.
- K001717: Micor Conduction Catheter, Micor, Inc. (2000)
- K003966: Wundcath Conduction Catheter, Micor, Inc. (2001)
- K003611: Pain Care Multi-Port Catheter, Model 2000L, Breg, Inc. (2000)

## Most influential descendants
- K060119: Mckinley Saturation Catheter (2006), 0 descendants of its own

## Indications for use
The Conduction Catheter is intended for administration of local anesthetics into intra-operative sites for post-operative pain management and for regional anesthesia outside of the epidural space. Routes of administration may be intra-operative, subcutaneous or percutaneous.

Source page: https://510kreport.com/device/K031600
Methodology: https://510kreport.com/methodology