KERR HERCULITE DENTAL COMPOSITE RESTORATIVE MATERI— 510(k) K844662

Name: FDA 510(k) clearance K844662
Creator: U.S. Food and Drug Administration
Published: 1985-03-25

Substantially Equivalent

Kerr Corporation (Danbury)

FDA 510(k) clearance K844662 for KERR HERCULITE DENTAL COMPOSITE RESTORATIVE MATERI, Substantially Equivalent on 1985-03-25. Applicant: Kerr Corporation (Danbury). Device class: 2.

Clearance details

Applicant: Kerr Corporation (Danbury)
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 1984-11-30
Decision date: 1985-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.