# K001717: Micor Conduction Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Micor, Inc.
- Decided: Sep 20, 2000 after 107 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
No predicates in its family tree.
5 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K093920: Busse Epidural Catheter Kit (2010), 2 descendants of its own
- 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
- K031600: Conduction Catheter (2003), 1 descendant of its own
- K201031: NRFit® Caps, Male and Female Neuraxial Tip Caps (2020), 0 descendants of its own
- K060119: Mckinley Saturation Catheter (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K001717
Methodology: https://510kreport.com/methodology