FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Intri26 Introducer Sheath

K Number: K252508 · Decision Dec 17, 2025
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
30
Review Days
131

Basic Information

Device Name
Intri26 Introducer Sheath
K Number
K252508
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Inari Medical, Inc.
Date Received
August 8, 2025
Decision Date
December 17, 2025
Product Code
DYB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DYB Introducer, Catheter

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