KERR OPTIBOND, MODIFICATION— 510(k) K934690

Name: FDA 510(k) clearance K934690
Creator: U.S. Food and Drug Administration
Published: 1993-12-30

Substantially Equivalent

Kerr Corporation (Danbury)

FDA 510(k) clearance K934690 for KERR OPTIBOND, MODIFICATION, Substantially Equivalent on 1993-12-30. Applicant: Kerr Corporation (Danbury). Device class: 2.

Clearance details

Applicant: Kerr Corporation (Danbury)
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 1993-07-26
Decision date: 1993-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Romulus, MI, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.