FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

DTX Studio Clinic 3.0

K Number: K213562 · Decision Mar 25, 2022
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
92
Review Days
136

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Basic Information

Device Name
DTX Studio Clinic 3.0
K Number
K213562
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nobel Biocare AB
Date Received
November 9, 2021
Decision Date
March 25, 2022
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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