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

DIAGNOCAM

K Number: K123402 · Decision Sep 24, 2013
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
10
Applicant Total
9
Review Days
323

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Basic Information

Device Name
DIAGNOCAM
K Number
K123402
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1745
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kaltenbach & Voigt GmbH
Date Received
November 5, 2012
Decision Date
September 24, 2013
Product Code
NTK
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
NTK Caries Detector, Laser Light, Transmission

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K140308 MASTERSURG / EXPERTSURG
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K103027 ELECTROTORQUE TLC