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

3M Filtek Universal Restorative

K Number: K183476 · Decision Jan 2, 2019
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
12
Review Days
16

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Basic Information

Device Name
3M Filtek Universal Restorative
K Number
K183476
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3M Espe Dental Products
Date Received
December 17, 2018
Decision Date
January 2, 2019
Product Code
EBF
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
Y

Classifications

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

Product Code Device Name
EBF Material, Tooth Shade, Resin

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