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

CERA R PLUS ALLOY

K Number: K032319 · Decision Sep 30, 2003
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
626
Applicant Total
23
Review Days
64

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Basic Information

Device Name
CERA R PLUS ALLOY
K Number
K032319
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3060
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply International
Date Received
July 28, 2003
Decision Date
September 30, 2003
Product Code
EJT
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
EJT Alloy, Gold-Based Noble Metal

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