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

SureWave Elastography (Q7000225)

K Number: K242006 · Decision Feb 12, 2025
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
21
Review Days
218

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Basic Information

Device Name
SureWave Elastography (Q7000225)
K Number
K242006
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quality Electrodynamics, LLC
Date Received
July 9, 2024
Decision Date
February 12, 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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K173469 16ch T/R Hand Wrist Coil
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K162946 8ch Knee-Foot SPEEDER
K162623 16ch T/R Hand Wrist Coil
K162966 TxRx Knee 15 Flare MR Coil 1.5T
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