# K885278: Epidural Anesthesia Tray

- Pathway: 510(k) (Traditional)
- Applicant: Preferred Medical Products
- Decided: Mar 16, 1989 after 83 days
- Product code: CAZ (Anesthesia Conduction Kit)
- Device class: 2
- Regulation: 21 CFR 868.5140
- 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; 1 cites 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
- K991879: Spring-Wound Epidural Catheter (1999), 4 descendants of its own
- K031600: Conduction Catheter (2003), 1 descendant of its own
- K231242: Perifix FX Catheter; Contiplex FX Catheter (2023), 0 descendants of its own
- K060119: Mckinley Saturation Catheter (2006), 0 descendants of its own
- K050557: Amt Nanocath (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K885278
Methodology: https://510kreport.com/methodology