# K960806: Turbo Tracker

- Pathway: 510(k) (Traditional)
- Applicant: Target Therapeutics
- Decided: May 2, 1996 after 64 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
186 later devices descend from it; 8 cite it directly.
0 of 187 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) Target Therapeutics’ Hydrophilic Tracker Infusion Catheter: named in the summary without a submission number

## Most influential descendants
- K994155: Excelsior 1018 Microcatheter (2000), 120 descendants of its own
- K013789: Excelsior SL-10 Microcatheter, Models 168581, 168381, 168181, 168189 (2001), 81 descendants of its own
- K030637: Ekos Peripheral Infusion System (2003), 50 descendants of its own
- K033214: Ekos Peripheral Infusion System (2003), 46 descendants of its own
- K083343: Headway 17 Microcatheter (2008), 39 descendants of its own

## Indications for use
TurboTRACKERS are intended to assist in the delivery of diagnostic agents such as contrast media and therapeutic agents such as occlusion coils into the peripheral, coronary, and neuro vasculature.

Source page: https://510kreport.com/device/K960806
Methodology: https://510kreport.com/methodology