VERACAM— 510(k) K021083

Substantially Equivalent

Lumalite, Inc.

FDA 510(k) clearance K021083 for VERACAM, Substantially Equivalent on 2002-08-30. Applicant: Lumalite, Inc.. Device class: 1.

Clearance details

Applicant: Lumalite, Inc.
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 2002-04-03
Decision date: 2002-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, 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.