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

RADIOPAQUE, GLASS IONOMER ENDODONTIC CEMENT

K Number: K042215 · Decision Sep 21, 2004
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
41
Review Days
36

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Basic Information

Device Name
RADIOPAQUE, GLASS IONOMER ENDODONTIC CEMENT
K Number
K042215
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Premier Dental Products Co.
Date Received
August 16, 2004
Decision Date
September 21, 2004
Product Code
EMA
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
EMA Cement, Dental

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K131212 PREMIER CERAMIC PRIMER
K083695 TRAXODENT
K062683 ENAMEL PRO VARNISH
K062166 ENAMEL PRO
K061997 PREMIER SELF-ETCHING ENAMEL SEALANT
K061998 PREMIER SELF-ETCHING BOND ENHANCER
K051866 PREMIER TEMPORARY CEMENT
K033309 PREMIER IMPLANT CEMENT, MODEL 3001450
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