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

X-MIND UNITY

K Number: K132378 · Decision May 30, 2014
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
189
Applicant Total
5
Review Days
303

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Basic Information

Device Name
X-MIND UNITY
K Number
K132378
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
De Gotzen S.R.L.
Date Received
July 31, 2013
Decision Date
May 30, 2014
Product Code
EHD
Advisory Committee
Dental
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
EHD Unit, X-Ray, Extraoral With Timer

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Other Clearances by De Gotzen S.R.L.

K Number Device Name
K201382 X-MIND prime 3D (under trademark Acteon), I-MAX 3D (under trademark Owandy Radiology)
K191719 X-MIND Trium
K192165 Acteon Imaging Suite
K160166 X-MIND trium