FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FLUOR PROTECTOR S

K Number: K131487 · Decision Oct 8, 2014
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
137
Applicant Total
31
Review Days
503

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Basic Information

Device Name
FLUOR PROTECTOR S
K Number
K131487
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 23, 2013
Decision Date
October 8, 2014
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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