FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

LC PROVIFILL

K Number: K010012 · Decision Feb 14, 2001
Classifications
1
FEI Numbers
183
Registration Numbers
183
Same Product Code
186
Applicant Total
20
Review Days
43

Basic Information

Device Name
LC PROVIFILL
K Number
K010012
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3770
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
S & C POLYMER GMBH
Date Received
January 2, 2001
Decision Date
February 14, 2001
Product Code
EBG
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
EBG Crown And Bridge, Temporary, Resin

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K081702 CARBOXYLATE CEM, PHOSPHATE CEM
K042614 S&C-SELF ETCH PR-BOND
K031420 S & C -BRACKET ADHESIVES
K012767 S & C HYDRO VINYL POLYSILOXANE IMPRESSION MATERIAL
K011277 HARD RELINER
K011431 RESIN CEM
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