Class Class II

Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging Catheter (K242966)

K242966 2025-01-31 Traditional
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Description

Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging Catheter by Gentuity, LLC, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242966
Clearance Date2025-01-31
Clearance TypeTraditional
Product CodeDQO
Regulation Number870.1200

Categories

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Predicate lineage for K242966

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging Catheter (K242966) cites 1 predicate device and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K242239HF-OCT Imaging System with Vis-RX Micro-Imaging Catheter (G...Gentuity, LLC2024

Trace the full predicate network for K242966

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

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