FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

X-View 3D Pan/X-View 2D Pan

K Number: K222666 · Decision Jul 10, 2023
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
5
Review Days
307

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Basic Information

Device Name
X-View 3D Pan/X-View 2D Pan
K Number
K222666
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Trident S.R.L
Date Received
September 6, 2022
Decision Date
July 10, 2023
Product Code
OAS
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
OAS X-Ray, Tomography, Computed, Dental

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