FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

Deep Learning Image Reconstruction

K Number: K193170 · Decision Dec 13, 2019
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
10
Review Days
28

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Basic Information

Device Name
Deep Learning Image Reconstruction
K Number
K193170
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Healthcare Japan Corporation
Date Received
November 15, 2019
Decision Date
December 13, 2019
Product Code
JAK
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
JAK System, X-Ray, Tomography, Computed

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