# K203623: StentBoost Mobile

- Pathway: 510(k) (Abbreviated)
- Applicant: Philips India Limited
- Decided: Apr 5, 2021 after 115 days
- Product code: OWB (Interventional Fluoroscopic X-Ray System)
- Device class: 2
- Regulation: 21 CFR 892.1650
- 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 K132305 (2013). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132305: Stentboost Rel. 4, Philips Medical Systems Nederland B.V. (2013) Summary page 7.

## Indications for use
StentBoost Mobile is intended for use as a vascular x-ray interventional application. StentBoost Mobile provides high image quality visualization of stents in relation to vessels. StentBoost Mobile assists in the treatment of endovascular diseases by visualizing the placement and deployment of stents.

Source page: https://510kreport.com/device/K203623
Methodology: https://510kreport.com/methodology