Atlas FDA

CHIKAI Nexus petit

FDA 510(k) clearance K252011 · decided 2026-02-02

Clearance details

K-number
K252011
Device name
CHIKAI Nexus petit
Applicant
Asahi Intecc Co., Ltd.
Decision
Substantially Equivalent
Date received
2025-06-27
Decision date
2026-02-02
Days to decision
220 days
Clearance type
Traditional
Product code
MOF
Device class
2
Regulation number
870.1330
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Seto, JP
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Aristotle Mini Guidewire (K260223)Scientia Vascular, Inc.2026-08-06
Drivewire 35 Guidewire (K254006)Rapid Medical Ltd.2026-07-17
Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom Wire 14 Guidewire (K253579)Scientia Vascular, Inc.2026-04-29
Zenith Micro Guidewire (K252317)Suzhou Zenith Vascular SciTech Limited2026-04-16
Willow 24 Guidewire (K260537)Arbor Endovascular, LLC2026-03-19
DCwire Micro-guidewire (K252122)Shanghai Achieva Medical Suzhou Co., Ltd.2026-03-16
Willow 18 Guidewire (K260130)Arbor Endovascular, LLC2026-02-13
0.014” Willow Guidewire (K253168)Arbor Endovascular, LLC2025-11-26
X-Wire Guidewire (K244061)Imperative Care, Inc.2025-08-26
0.014” Willow Guidewire (K243756)Arbor Endovascular, LLC2025-07-17
CHIKAI Nexus 014 (K243383)Asahi Intecc Co., Ltd.2025-04-21
Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom Wire 14 Guidewire; Aristotle Colossus Guidewire (K243938)Scientia Vascular, Inc.2025-04-01

Recalls involving this device

No recalls on record reference this clearance.