# K010707: Atlantis SR Plus Coronary Imaging Catheter, Model 35975

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific, Target
- Decided: Mar 29, 2001 after 20 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.
12 later devices descend from it; 1 cites it directly.
0 of 13 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
- K093857: C7 XR Imaging System with C7 Dragonfly Imaging Catheter and Disposable Accessories (2010), 11 descendants of its own
- K140185: Ocelot Catheter, Ocelot Pixl Catheter, Lightbox Console (2014), 7 descendants of its own
- K152275: Pantheris System (2015), 6 descendants of its own
- K153460: Pantheris Catheter (8Fr), Pantheris Catheter (7Fr) (2016), 5 descendants of its own
- K160827: Pantheris Catheter (2016), 4 descendants of its own

Source page: https://510kreport.com/device/K010707
Methodology: https://510kreport.com/methodology