CONTEC DUO, CONTEC LC, CONTEC LCR— 510(k) K030644

Substantially Equivalent

Dentaurum

FDA 510(k) clearance K030644 for CONTEC DUO, CONTEC LC, CONTEC LCR, Substantially Equivalent on 2003-11-21. Applicant: Dentaurum. Device class: 2.

Clearance details

Applicant: Dentaurum
Product code: Code DYH
Device class: Class 2
Regulation: 21 CFR 872.3750
Advisory panel: Dental
Date received: 2003-02-28
Decision date: 2003-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newtown, PA, 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.