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

ALEXANDER

K Number: K032493 · Decision Sep 4, 2003
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
626
Applicant Total
62
Review Days
23

Basic Information

Device Name
ALEXANDER
K Number
K032493
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3060
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
IVOCLAR VIVADENT, INC.
Date Received
August 12, 2003
Decision Date
September 4, 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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K103556 IPS E.MAX CAD CRYSTALL / CONNECT AND IPS E.MAX CAD CRYSTAL / ADD-ON CONNECT (FOR CAD-ON TECHNIQUE)
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K103379 TELIO CS INLAY & TELIO CS ONLAY
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