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

Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20)

K Number: K242841 · Decision May 27, 2025
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
62
Applicant Total
44
Review Days
250

Basic Information

Device Name
Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20)
K Number
K242841
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4725
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Medical
Date Received
September 19, 2024
Decision Date
May 27, 2025
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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