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

IBOND GLUMA INSIDE

K Number: K022612 · Decision Oct 28, 2002
Classifications
1
FEI Numbers
133
Registration Numbers
133
Same Product Code
410
Applicant Total
145
Review Days
83

Basic Information

Device Name
IBOND GLUMA INSIDE
K Number
K022612
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
HERAEUS KULZER, INC.
Date Received
August 6, 2002
Decision Date
October 28, 2002
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

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