# K990271: Endosonics Trak Back Device

- Pathway: 510(k) (Traditional)
- Applicant: Endosonics Corp.
- Decided: Aug 30, 1999 after 214 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- 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. The FDA summary names its predicate without a number.
- (no number) EndoSonics Automatic Pull Back Device: named in the summary without a submission number
- (no number) CVIS Catheter Pull-Back Device: named in the summary without a submission number
- (no number) Intertherapy Interpret Catheter Linear Translator: named in the summary without a submission number

## Most influential descendants
- K021802: Stereotaxis Catheter Advancer System (2003), 2 descendants of its own
- K042850: Cardiodrive, Model 001-004115 (Non-Sterile); 001-1169-1 (Sterile) (2006), 0 descendants of its own
- K051374: Cardiodrive Catheter Advancement System (2005), 0 descendants of its own

## Indications for use
The Trak Back can be used with the Visions Five-64 series ultrasound imaging catheter. The Trak Back withdraws the imaging catheter from the vessel through the guide catheter.

Source page: https://510kreport.com/device/K990271
Methodology: https://510kreport.com/methodology