# K983125: Epidural Catheter Models 1210/1200

- Pathway: 510(k) (Traditional)
- Applicant: Rusch Intl.
- Decided: Nov 17, 1998 after 70 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
Longest line of descent: 1 generation back to K840201 (1984). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K840201: Epidural Catheter Tray, Aries Medical, Inc. (1984) Summary page 1.

## Indications for use
To administer to a patient conduction, regional, or local anesthesia.

Source page: https://510kreport.com/device/K983125
Methodology: https://510kreport.com/methodology