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

ENDOREZ

K Number: K992097 · Decision Oct 26, 1999
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
142
Applicant Total
103
Review Days
127

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Basic Information

Device Name
ENDOREZ
K Number
K992097
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3820
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ultradent Products, Inc.
Date Received
June 21, 1999
Decision Date
October 26, 1999
Product Code
KIF
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
KIF Resin, Root Canal Filling

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