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

SonialVision G4

K Number: K190373 · Decision Mar 15, 2019
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
9
Review Days
24

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Basic Information

Device Name
SonialVision G4
K Number
K190373
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shimadzu Corporation
Date Received
February 19, 2019
Decision Date
March 15, 2019
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

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K152244 RADspeed Pro
K123508 TRINIAS