# K023907: Cordis Maxi LD Large Diameter Balloon Dilatation Catheter, Cordis Maxi LD Pta Balloon Dilation Catheter

- Pathway: 510(k) (Special)
- Applicant: Cordis Corp.
- Decided: Dec 18, 2002 after 23 days
- Product code: KNQ (Dilator, Esophageal)
- Device class: 2
- Regulation: 21 CFR 876.5365
- 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 K993720 (2000). 1 ancestor in all.
52 later devices descend from it; 2 cite it directly.
0 of 54 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993720: Cordis Maxi LD Large Diameter Balloon Dilatation Catheter, Cordis Corp. (2000) Summary page 1.
- (no number) B. Braun IMPACT Balloon Dilatation Catheter: named in the summary without a submission number

## Most influential descendants
- K032587: Edwards Peripheral Dilatation Catheter (2003), 48 descendants of its own
- K052149: Edwards Peripheral Dilation Catheter (2005), 47 descendants of its own
- K083657: Conquest Pta Balloon Dilatation Catheter (2008), 44 descendants of its own
- K103459: Vascutrak Pta Dilatation Catheter (2010), 36 descendants of its own
- K112182: Angiosculpt Pta Scoring Balloon Catheter (2011), 29 descendants of its own

## Indications for use
The Cordis Maxi LD Large Balloon Dilatation Catheter is intended for use in the dilatation of strictures of the esophagus.

Source page: https://510kreport.com/device/K023907
Methodology: https://510kreport.com/methodology