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

visor2 system

K Number: K210109 · Decision Apr 8, 2022
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
8
Review Days
444

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Basic Information

Device Name
visor2 system
K Number
K210109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eemagine Medical Imaging Solutions GmbH
Date Received
January 19, 2021
Decision Date
April 8, 2022
Product Code
HAW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HAW Neurological Stereotaxic Instrument

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K070358 MAXINSIGHT
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K002631 ELECTROENCEPHALOGRAPH SOFTWARE EEMAGINE EEG