# K924541: Epidural Minipack

- Pathway: 510(k) (Traditional)
- Applicant: Concord/Portex
- Decided: Jul 9, 1993 after 304 days
- Product code: BYO (Bottle, Blow)
- Device class: 1
- Regulation: 21 CFR 868.5220
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K033080: Portex 24G Pediatric Epidural and Peripheral Block Anesthesia Catheter (2004), 2 descendants of its own
- K062902: Pajunks Epilong Set Pediatric (2007), 1 descendant of its own
- K090884: Perifix One Pediatric Catheter, 20 GA. & 24 GA. (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K924541
Methodology: https://510kreport.com/methodology