FDA 510(k) FDA class 1 Substantially Equivalent 🇩🇪 Germany

MASTERTORQUE LUX 8900 L

K Number: K130560 · Decision Sep 27, 2013
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
260
Applicant Total
9
Review Days
207

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Basic Information

Device Name
MASTERTORQUE LUX 8900 L
K Number
K130560
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kaltenbach & Voigt GmbH
Date Received
March 4, 2013
Decision Date
September 27, 2013
Product Code
EFB
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
EFB Handpiece, Air-Powered, Dental

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