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

STAR RF Ablation System

K Number: K251802 · Decision Feb 13, 2026
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
65
Applicant Total
178
Review Days
246

Basic Information

Device Name
STAR RF Ablation System
K Number
K251802
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4725
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Merit Medical Systems, Inc.
Date Received
June 12, 2025
Decision Date
February 13, 2026
Product Code
GXI
Advisory Committee
Neurology
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
GXI Probe, Radiofrequency Lesion

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