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

SOLOBOND PLUS

K Number: K003153 · Decision Nov 15, 2000
Classifications
1
FEI Numbers
133
Registration Numbers
133
Same Product Code
410
Applicant Total
94
Review Days
36

Basic Information

Device Name
SOLOBOND PLUS
K Number
K003153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
VOCO GMBH
Date Received
October 10, 2000
Decision Date
November 15, 2000
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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