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

PREMISE MODIFIED

K Number: K090292 · Decision Apr 3, 2009
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
9
Review Days
57

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Basic Information

Device Name
PREMISE MODIFIED
K Number
K090292
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kerr Corp.
Date Received
February 5, 2009
Decision Date
April 3, 2009
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

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Other Clearances by Kerr Corp.

K Number Device Name
K091613 TAKE 1
K081695 DMC COMPOSITE
K072622 STANDOUT 2
K042888 DEMETRON IDS CURING LIGHT
K031484 STAND OUT
K014179 DEMETRON LC
K010994 TAKE ONE BITE MODIFIED
K001655 PERMLASTIC 2