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

14Fr Low Profile Introducer Kit

K Number: K252766 · Decision Oct 8, 2025
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
19
Review Days
40

Basic Information

Device Name
14Fr Low Profile Introducer Kit
K Number
K252766
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abiomed, Inc.
Date Received
August 29, 2025
Decision Date
October 8, 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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