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

Sonic DL

K Number: K243667 · Decision Jun 5, 2025
Classifications
1
FEI Numbers
152
Registration Numbers
152
Same Product Code
1071
Applicant Total
25
Review Days
190

Basic Information

Device Name
Sonic DL
K Number
K243667
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Medical Systems, LLC
Date Received
November 27, 2024
Decision Date
June 5, 2025
Product Code
LNH
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LNH System, Nuclear Magnetic Resonance Imaging

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