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

IPS INLINE POM SYSTEM

K Number: K071848 · Decision Aug 30, 2007
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
471
Applicant Total
62
Review Days
56

Basic Information

Device Name
IPS INLINE POM SYSTEM
K Number
K071848
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
IVOCLAR VIVADENT, INC.
Date Received
July 5, 2007
Decision Date
August 30, 2007
Product Code
EIH
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
EIH Powder, Porcelain

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