OrthoPulse— 510(k) K143120

Substantially Equivalent

Biolux Research , Ltd.

FDA 510(k) clearance K143120 for OrthoPulse, Substantially Equivalent on 2015-07-24. Applicant: Biolux Research , Ltd..

Clearance details

Applicant: Biolux Research , Ltd.
Product code: Code PLH
Advisory panel: Dental
Date received: 2014-10-30
Decision date: 2015-07-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vancouver, CA

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