LINER, CAVITY CALCIUM HYDROXIDE— 510(k) K781688

Name: FDA 510(k) clearance K781688
Creator: U.S. Food and Drug Administration
Published: 1978-12-20

Substantially Equivalent

Kerr Corporation (Danbury)

FDA 510(k) clearance K781688 for LINER, CAVITY CALCIUM HYDROXIDE, Substantially Equivalent on 1978-12-20. Applicant: Kerr Corporation (Danbury). Device class: 2.

Clearance details

Applicant: Kerr Corporation (Danbury)
Product code: Code EJK
Device class: Class 2
Regulation: 21 CFR 872.3250
Advisory panel: Dental
Date received: 1978-10-04
Decision date: 1978-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.