FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

CHIKAI Nexus petit

K Number: K252011 · Decision Feb 2, 2026
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
39
Applicant Total
84
Review Days
220

Basic Information

Device Name
CHIKAI Nexus petit
K Number
K252011
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Asahi Intecc Co., Ltd.
Date Received
June 27, 2025
Decision Date
February 2, 2026
Product Code
MOF
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOF Guide, Wire, Catheter, Neurovasculature

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