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

dS FootAnkle 16Ch Coils for 1.5T and 3.0T, dS HiRes HandWrist 16Ch Coils for 1.5T and 3.0T, ds Small Extremity 16Ch Coils for 1.5T and 3.0T

K Number: K213766 · Decision Dec 23, 2021
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
29
Review Days
22

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Basic Information

Device Name
dS FootAnkle 16Ch Coils for 1.5T and 3.0T, dS HiRes HandWrist 16Ch Coils for 1.5T and 3.0T, ds Small Extremity 16Ch Coils for 1.5T and 3.0T
K Number
K213766
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Invivo Corporation
Date Received
December 1, 2021
Decision Date
December 23, 2021
Product Code
MOS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

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

Product Code Device Name
MOS Coil, Magnetic Resonance, Specialty

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