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

EVERBOND GLASS IONOMER CEMENT

K Number: K823795 · Decision Jan 26, 1983
Classifications
1
FEI Numbers
142
Registration Numbers
142
Same Product Code
495
Applicant Total
37
Review Days
30

Basic Information

Device Name
EVERBOND GLASS IONOMER CEMENT
K Number
K823795
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
SYBRON CORP.
Date Received
December 27, 1982
Decision Date
January 26, 1983
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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