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

TYPE 1 DENTAL CEMENT

K Number: K921173 · Decision Nov 4, 1992
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
47
Review Days
238

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Basic Information

Device Name
TYPE 1 DENTAL CEMENT
K Number
K921173
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Centrix, Inc.
Date Received
March 11, 1992
Decision Date
November 4, 1992
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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