OPTIBOND ALL-IN-ONE— 510(k) K060469

Name: FDA 510(k) clearance K060469
Creator: U.S. Food and Drug Administration
Published: 2006-03-28

Substantially Equivalent

Sybron Dental Specialties, Inc.

FDA 510(k) clearance K060469 for OPTIBOND ALL-IN-ONE, Substantially Equivalent on 2006-03-28. Applicant: Sybron Dental Specialties, Inc.. Device class: 2.

Clearance details

Applicant: Sybron Dental Specialties, Inc.
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 2006-02-23
Decision date: 2006-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newport Beach, CA, US

Download summary PDF View on FDA.gov ↗

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