FDA 510(k) FDA class 2 Substantially Equivalent 🇱🇮 Liechtenstein

Cervitec F

K Number: K191453 · Decision Feb 11, 2020
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
137
Applicant Total
31
Review Days
256

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Basic Information

Device Name
Cervitec F
K Number
K191453
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3260
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ivoclar Vivadent, AG
Date Received
May 31, 2019
Decision Date
February 11, 2020
Product Code
LBH
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
LBH Varnish, Cavity

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