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

Agilis NxT Steerable Introducer Dual-Reach

K Number: K243493 · Decision Dec 13, 2024
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
57
Review Days
31

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Basic Information

Device Name
Agilis NxT Steerable Introducer Dual-Reach
K Number
K243493
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ABBOTT MEDICAL
Date Received
November 12, 2024
Decision Date
December 13, 2024
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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