Class Class II

CHIKAI Nexus 014 (K243383)

K243383 2025-04-21 Traditional
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Description

CHIKAI Nexus 014 by Asahi Intecc Co., Ltd., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243383
Clearance Date2025-04-21
Clearance TypeTraditional
Product CodeMOF
Regulation Number870.1330

Categories

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Predicate lineage for K243383

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. CHIKAI Nexus 014 (K243383) cites 5 predicate devices and is itself cited by 1 later device.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K191714ASAHI Neurovascular Guide Wire CHIKAI X 014 softAsahi Intecc Co., Ltd.2019
K163426ASAHI PTCA, Peripheral, and Neurovascular Guide Wires, ASAH...Asahi Intecc Co., Ltd.2017
K160659ASAHI CHIKAI Neurovascular Guide Wire (Round Curve)Asahi Intecc Co., Ltd.2016
K141751ASAHI NEUROVASCULAR GUIDE WIRE ASAHI CHIKAI 008, ASAHI NEUR...Asahi Intecc Co., Ltd.2015
K022762JOWIRE NEO'S PTCA CATHETER GUIDEWIRES, MODELS AG141000, AG1...Jomed, Inc.2002

Later devices that cite this one as their predicate

Devices that cite K243383
K numberDeviceApplicantYear
K243382RZ Resectoscope SystemRz Medizintechnik GmbH2025

Trace the full predicate network for K243383

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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