# K850505: Deseret Epidural Catheter W/Toughy-Borst Adapter

- Pathway: 510(k) (Traditional)
- Applicant: Parke-Davis Co.
- Decided: Mar 11, 1985 after 31 days
- Product code: BSO (Catheter, Conduction, Anesthetic)
- Device class: 2
- Regulation: 21 CFR 868.5120
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Nov 17, 2005 · Not classified · Z-0467-06: The catheter connector could not be sufficiently tightened to secure the catheter tubing.
- Nov 17, 2005 · Not classified · Z-0468-06: The catheter connector could not be sufficiently tightened to secure the catheter tubing.

Source page: https://510kreport.com/device/K850505
Methodology: https://510kreport.com/methodology