VENEER SYSTEM, MOSTIQUE LAMINATE— 510(k) K782080

Name: FDA 510(k) clearance K782080
Creator: U.S. Food and Drug Administration
Published: 1979-01-26

Substantially Equivalent

Caulk Co., Div. Dentsply

FDA 510(k) clearance K782080 for VENEER SYSTEM, MOSTIQUE LAMINATE, Substantially Equivalent on 1979-01-26. Applicant: Caulk Co., Div. Dentsply. Device class: 2.

Clearance details

Applicant: Caulk Co., Div. Dentsply
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 1978-12-13
Decision date: 1979-01-26
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.