FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

SIDEXIS 4

K Number: K132773 · Decision Dec 11, 2013
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
38
Review Days
97

Basic Information

Device Name
SIDEXIS 4
K Number
K132773
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SIRONA DENTAL SYSTEMS GMBH
Date Received
September 5, 2013
Decision Date
December 11, 2013
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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